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

rs797045116

From SNPedia

ClinVar
Risk rs797045116(A;A)
Alt rs797045116(A;A)
Reference rs797045116(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCM
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.45628393dupA
CLNSRC
CLNACC RCV000190644.1,