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rs1064795675

From SNPedia
ClinVar
Risk rs1064795675(TGT;TGT)
Alt rs1064795675(TGT;TGT)
Reference Rs1064795675(GGCCGGAAGATG;GGCCGGAAGATG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C11orf65 ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108235876_108235887delGGCCGGAAGATGinsTGT
CLNSRC
CLNACC RCV000481418.1,