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rs761695866

From SNPedia

ClinVar
Risk rs761695866(C;C)
Alt rs761695866(C;C)
Reference rs761695866(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.64572091dupC
CLNSRC
CLNACC RCV000182442.1,