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rs587782847

From SNPedia

ClinVar
Risk rs587782847(;)
Alt rs587782847(;)
Reference rs587782847(GAAACTGAAAG;GAAACTGAAAG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108236111_108236121delAACTGAAAGGA
CLNSRC
CLNACC RCV000132441.2,