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rs863223291

From SNPedia

ClinVar
Risk rs863223291(;)
Alt rs863223291(;)
Reference rs863223291(ACAAGCT;ACAAGCT)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene ROR2
CLNDBN Robinow syndrome, autosomal recessive
Reversed 1
HGVS NC_000009.11:g.94486833_94486839delAGCTTGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007737.3,