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rs1064792949

From SNPedia
ClinVar
Risk rs1064792949(-;-)
Alt rs1064792949(-;-)
Reference Rs1064792949(GGACAAAAGGCA;GGACAAAAGGCA)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131973909_131973920delACAAAAGGCAGG
CLNSRC
CLNACC RCV000464633.1,