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rs778390089

From SNPedia

ClinVar
Risk rs778390089(;)
Alt rs778390089(;)
Reference rs778390089(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene TRPM1
CLNDBN Congenital stationary night blindness, type 1C
Reversed 0
HGVS NC_000015.9:g.31318400delC
CLNSRC
CLNACC RCV000176649.1,