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rs587782866

From SNPedia

ClinVar
Risk rs587782866(;)
Alt rs587782866(;)
Reference rs587782866(TTCCTGTGTCAGATA;TTCCTGTGTCAGATA)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131973763_131973777delCCTGTGTCAGATATT
CLNSRC
CLNACC RCV000132490.1,