ClinVar Miner

List of variants reported as uncertain significance for congenital stationary night blindness 1B

Included ClinVar conditions (1):

Congenital stationary night blindness 1B

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.1537G>A (p.Val513Met)	rs201396068	0.00012
NM_000843.4(GRM6):c.2240C>T (p.Ser747Leu)	rs759761288	0.00003
NM_000843.4(GRM6):c.824G>A (p.Gly275Asp)

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