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rs796051861

From SNPedia

ClinVar
Risk
Alt
Reference Rs796051861(C;C)
Significance Pathogenic
Disease Usher syndrome USHER SYNDROME Usher syndrome not provided
Variation info
Gene LOC102723377 CDH23
CLNDBN Usher syndrome, type 1D USHER SYNDROME, TYPE ID/F, DIGENIC Usher syndrome, type 1 not provided
Reversed 0
HGVS NC_000010.10:g.73269886delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000005207.4, RCV000005208.4, RCV000215123.1, RCV000254862.1,