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Ophthalmology Eyes Vision Panel NGS Genetic DNA Test Cost 20000 Rs
Ophthalmology Eyes Vision Panel NGS Genetic DNA Test Details
List of genes tested using NGS technology for detection of variant and mutation in Ophthalmology Eyes Vision Panel are ABCA4, ABCB6, ABHD12, ACO2, ACVR1, ADAM9, ADGRV1, AFG3L2, AGK, AHI1, AIPL1, ALDH18A1, ALDH1A3, AP3B1, APTX, ARL13B, ARL6, ASB10, ATF6, AUH, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BEST1, BFSP1, BFSP2, BLOC1S3, BLOC1S6, BMP4, C12orf65, C1QTNF5, C8orf37, CA4, CABP4, CACNA1F, CACNA2D4, CANT1, CC2D2A, CCDC28B, CDH23, CDH3, CDHR1, CEP164, CEP290, CEP41, CERKL, CHD7, CHM, CHMP4B, CIB2, CISD2, CLCN7, CLN3, CLN5, CLN6, CLN8, CLPB, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CNNM4, COL11A1, COL11A2, COL2A1, COL4A1, COL9A1, COL9A2, COL9A3, COX7B, CPLANE1, CRB1, CRX, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGB, CRYGC, CRYGD, CRYGS, CSPP1, CTC1, CTDP1, CTNNB1, CTSD, CYP1B1, CYP27A1, DGUOK, DHDDS, DKC1, DNA2, DNAJC19, DNM1L, DTNBP1, EDN3, EDNRB, EFEMP1, ELOVL4, ENPP1, EPHA2, ERCC1, ERCC2, ERCC5, ERCC6, EYA1, EYS, FAM126A, FAM161A, FLVCR1, FOXC1, FOXE3, FOXL2, FRAS1, FREM1, FREM2, FSCN2, FTL, FYCO1, FZD4, GALE, GALK1, GALT, GBA, GCNT2, GDF3, GDF6, GJA1, GJA3, GJA8, GNAT2, GNPTG, GPR143, GRIP1, GRN, GUCA1A, GUCA1B, GUCY2D, HCCS, HESX1, HEXA, HGSNAT, HK1, HMX1, HPS1, HPS3, HPS4, HPS5, HPS6, HSF4, HTRA2, IDH3B, IFT140, IFT172, IFT27, IMPDH1, IMPG2, INPP5E, IQCB1, KCNJ13, KCNV2, KIF11, KIF7, KIT, KLHL7, LCA5, LEMD2, LEP, LEPR, LIM2, LMX1B, LOXL1, LRAT, LRMDA, LRP2, LRP5, LSS, LTBP2, LYST, LZTFL1, MAB21L2, MAF, MAK, MC1R, MERTK, MFN2, MFRP, MFSD8, MIP, MITF, MKKS, MKS1, MLPH, MYH9, MYO5A, MYO7A, MYOC, NAA10, NDP, NF2, NHS, NMNAT1, NPHP1, NPHP3, NPHP4, NR0B2, NR2F1, NRL, NTF4, OCA2, OCRL, OFD1, OPA1, OPA3, OPN1LW, OPN1MW, OPTN, OSTM1, OTX2, P3H2, PAX2, PAX3, PAX6, PCARE, PCDH15, PDE6A, PDE6B, PDE6C, PDE6G, PDE6H, PDZD7, PEX1, PEX2, PEX7, PHF6, PHYH, PIK3R5, PITPNM3, PITX2, PITX3, PLA2G5, PNKP, PNPLA6, POLG, POLG2, POMC, POMGNT1, PPARG, PPT1, PQBP1, PRCD, PRKCG, PROM1, PRPF3, PRPF31, PRPF6, PRPF8, PRPH2, PRPS1, PRSS56, RAB18, RAB27A, RAB3GAP1, RAB3GAP2, RARB, RAX, RAX2, RBP3, RBP4, RD3, RDH12, RDH5, RGR, RGS9, RGS9BP, RHO, RIMS1, RLBP1, ROM1, RP1, RP1L1, RP2, RPE65, RPGR, RPGRIP1, RPGRIP1L, RRM2B, RS1, RTN4IP1, SAG, SBF2, SDCCAG8, SEMA4A, SERAC1, SETX, SHH, SIL1, SIX3, SIX6, SLC16A12, SLC24A5, SLC25A4, SLC25A46, SLC33A1, SLC45A2, SLC9A6, SMCHD1, SMOC1, SNAI2, SNRNP200, SNX10, SOX10, SOX2, SPATA7, SPG7, STRA6, TBC1D20, TBK1, TCIRG1, TCTN1, TCTN2, TCTN3, TDRD7, TENM3, TFAP2A, TIMM8A, TIMP3, TK2, TMEM126A, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TMEM70, TNFRSF11A, TNFSF11, TOPORS, TPP1, TRIM32, TRNT1, TSPAN12, TTC21B, TTC8, TTPA, TULP1, TWNK, TYMP, TYR, TYRP1, UNC45B, USH1C, USH1G, USH2A, VCAN, VIM, VPS13B, VSX2, WDPCP, WDR19, WDR36, WFS1, WHRN, ZIC2, ZNF423, ZNF513
Clinical History of Patient who is going for Ophthalmology Eyes Vision Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCA4, ABCB6, ABHD12, ACO2, ACVR1, ADAM9, ADGRV1, AFG3L2, AGK, AHI1, AIPL1, ALDH18A1, ALDH1A3, AP3B1, APTX, ARL13B, ARL6, ASB10, ATF6, AUH, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BEST1, BFSP1, BFSP2, BLOC1S3, BLOC1S6, BMP4, C12orf65, C1QTNF5, C8orf37, CA4, CABP4, CACNA1F, CACNA2D4, CANT1, CC2D2A, CCDC28B, CDH23, CDH3, CDHR1, CEP164, CEP290, CEP41, CERKL, CHD7, CHM, CHMP4B, CIB2, CISD2, CLCN7, CLN3, CLN5, CLN6, CLN8, CLPB, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CNNM4, COL11A1, COL11A2, COL2A1, COL4A1, COL9A1, COL9A2, COL9A3, COX7B, CPLANE1, CRB1, CRX, CRYAA, CRYAB, CRYBA1, CRYBA4, CRYBB1, CRYBB2, CRYBB3, CRYGB, CRYGC, CRYGD, CRYGS, CSPP1, CTC1, CTDP1, CTNNB1, CTSD, CYP1B1, CYP27A1, DGUOK, DHDDS, DKC1, DNA2, DNAJC19, DNM1L, DTNBP1, EDN3, EDNRB, EFEMP1, ELOVL4, ENPP1, EPHA2, ERCC1, ERCC2, ERCC5, ERCC6, EYA1, EYS, FAM126A, FAM161A, FLVCR1, FOXC1, FOXE3, FOXL2, FRAS1, FREM1, FREM2, FSCN2, FTL, FYCO1, FZD4, GALE, GALK1, GALT, GBA, GCNT2, GDF3, GDF6, GJA1, GJA3, GJA8, GNAT2, GNPTG, GPR143, GRIP1, GRN, GUCA1A, GUCA1B, GUCY2D, HCCS, HESX1, HEXA, HGSNAT, HK1, HMX1, HPS1, HPS3, HPS4, HPS5, HPS6, HSF4, HTRA2, IDH3B, IFT140, IFT172, IFT27, IMPDH1, IMPG2, INPP5E, IQCB1, KCNJ13, KCNV2, KIF11, KIF7, KIT, KLHL7, LCA5, LEMD2, LEP, LEPR, LIM2, LMX1B, LOXL1, LRAT, LRMDA, LRP2, LRP5, LSS, LTBP2, LYST, LZTFL1, MAB21L2, MAF, MAK, MC1R, MERTK, MFN2, MFRP, MFSD8, MIP, MITF, MKKS, MKS1, MLPH, MYH9, MYO5A, MYO7A, MYOC, NAA10, NDP, NF2, NHS, NMNAT1, NPHP1, NPHP3, NPHP4, NR0B2, NR2F1, NRL, NTF4, OCA2, OCRL, OFD1, OPA1, OPA3, OPN1LW, OPN1MW, OPTN, OSTM1, OTX2, P3H2, PAX2, PAX3, PAX6, PCARE, PCDH15, PDE6A, PDE6B, PDE6C, PDE6G, PDE6H, PDZD7, PEX1, PEX2, PEX7, PHF6, PHYH, PIK3R5, PITPNM3, PITX2, PITX3, PLA2G5, PNKP, PNPLA6, POLG, POLG2, POMC, POMGNT1, PPARG, PPT1, PQBP1, PRCD, PRKCG, PROM1, PRPF3, PRPF31, PRPF6, PRPF8, PRPH2, PRPS1, PRSS56, RAB18, RAB27A, RAB3GAP1, RAB3GAP2, RARB, RAX, RAX2, RBP3, RBP4, RD3, RDH12, RDH5, RGR, RGS9, RGS9BP, RHO, RIMS1, RLBP1, ROM1, RP1, RP1L1, RP2, RPE65, RPGR, RPGRIP1, RPGRIP1L, RRM2B, RS1, RTN4IP1, SAG, SBF2, SDCCAG8, SEMA4A, SERAC1, SETX, SHH, SIL1, SIX3, SIX6, SLC16A12, SLC24A5, SLC25A4, SLC25A46, SLC33A1, SLC45A2, SLC9A6, SMCHD1, SMOC1, SNAI2, SNRNP200, SNX10, SOX10, SOX2, SPATA7, SPG7, STRA6, TBC1D20, TBK1, TCIRG1, TCTN1, TCTN2, TCTN3, TDRD7, TENM3, TFAP2A, TIMM8A, TIMP3, TK2, TMEM126A, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TMEM70, TNFRSF11A, TNFSF11, TOPORS, TPP1, TRIM32, TRNT1, TSPAN12, TTC21B, TTC8, TTPA, TULP1, TWNK, TYMP, TYR, TYRP1, UNC45B, USH1C, USH1G, USH2A, VCAN, VIM, VPS13B, VSX2, WDPCP, WDR19, WDR36, WFS1, WHRN, ZIC2, ZNF423, ZNF513
Ophthalmology Eyes Vision Panel NGS Genetic DNA Test: Symptoms, Diagnosis, and Cost
Our eyes are one of the most important organs of our body, and our vision is essential for our daily lives. However, several genetic disorders can affect our eyes and vision, leading to various symptoms such as poor vision, blindness, and eye diseases. To diagnose these genetic disorders, ophthalmologists use a DNA test called the Ophthalmology Eyes Vision Panel NGS Genetic DNA Test.
Symptoms of Eye Genetic Disorders
Some of the common symptoms of eye genetic disorders are:
- Poor vision or blindness
- Eye pain or discomfort
- Drooping eyelids
- Cloudy or hazy vision
- Difficulty in seeing at night
- Color blindness
- Lazy eye
- Eye twitching or spasms
If you experience any of these symptoms, it is essential to consult an ophthalmologist who can recommend the appropriate tests and treatments.
Diagnosis of Eye Genetic Disorders
The Ophthalmology Eyes Vision Panel NGS Genetic DNA Test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the genetic material of a patient. This test can identify genetic mutations or abnormalities that may cause eye diseases or affect vision.
The test requires a small blood sample or a swab of the inside of the cheek. The sample is sent to a laboratory where it is analyzed using NGS technology. The results of the test can help ophthalmologists diagnose the underlying genetic disorder and recommend appropriate treatments.
Cost of Ophthalmology Eyes Vision Panel NGS Genetic DNA Test
The cost of the Ophthalmology Eyes Vision Panel NGS Genetic DNA Test in India is approximately INR 20,000. However, the cost may vary depending on the location of the laboratory and other factors.
Conclusion
The Ophthalmology Eyes Vision Panel NGS Genetic DNA Test is a valuable diagnostic tool that can help ophthalmologists diagnose genetic disorders that affect eyes and vision. If you experience any symptoms related to your eyes or vision, it is essential to consult an ophthalmologist who can recommend the appropriate tests and treatments.
At DNA Labs India, we offer a wide range of genetic tests, including the Ophthalmology Eyes Vision Panel NGS Genetic DNA Test. Our tests are accurate, reliable, and affordable. Contact us today to learn more about our services.
Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for Ophthalmology Eyes Vision Panel NGS Genetic DNA Test
