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

rs786203976

From SNPedia

ClinVar
Risk rs786203976(;)
Alt rs786203976(;)
Reference rs786203976(CTT;CTT)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108216629_108216631delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003154.3, RCV000167512.1,