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rs786204885

From SNPedia

ClinVar
Risk rs786204885(;)
Alt rs786204885(;)
Reference rs786204885(GCAAAAGCCGCA;GCAAAAGCCGCA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000010.10:g.89623031_89623042delAAGCCGCAGCAA
CLNSRC GeneDx
CLNACC RCV000129113.3, RCV000169826.2,