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rs397507753(TCAG;TCAG)

From SNPedia
common in clinvar
Is agenotype
ofrs397507753
GeneBRCA2
Chromosome13
Position32,339,342
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;GTCA) 6 BRCA2 variant considered pathogenic for breast cancer
(GTCA;GTCA) 0 common in clinvar
(TCAG;TCAG) 0 common in clinvar