ClinVar Miner

List of variants studied for retinal disorder by Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology

Included ClinVar conditions (500):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_006269.2(RP1):c.4636C>T (p.Gln1546Ter) rs1806147660

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