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rs794726667

From SNPedia

ClinVar
Risk rs794726667(A;A)
Alt rs794726667(A;A)
Reference rs794726667(;)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97864111dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012828.3,