Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776784

From SNPedia

ClinVar
Risk rs587776784(;)
Alt rs587776784(;)
Reference rs587776784(CTTGAATCTG;CTTGAATCTG)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027193_49027202delAATCTGCTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013957.2,