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rs786202318

From SNPedia
ClinVar
Risk rs786202318(-;-)
Alt rs786202318(-;-)
Reference Rs786202318(GAATGGTGCACAG;GAATGGTGCACAG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108213985_108213997delTGGTGCACAGGAA
CLNSRC
CLNACC RCV000165065.1, RCV000484455.1,