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rs786202264

From SNPedia

ClinVar
Risk rs786202264(;)
Alt rs786202264(;)
Reference rs786202264(ATGAAAGTCTCAA;ATGAAAGTCTCAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108190766_108190778delGAAAGTCTCAAAT
CLNSRC
CLNACC RCV000164992.1,