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rs796051866

From SNPedia

ClinVar
Risk rs796051866(;)
Alt rs796051866(;)
Reference rs796051866(CAAGTGCTGAAAT;CAAGTGCTGAAAT)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89938470_89938482delAAGTGCTGAAATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007206.5,