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rs397507602(TTCTG;TTCTG)

From SNPedia
common in clinvar
Is agenotype
ofrs397507602
GeneBRCA2
Chromosome13
Position32,333,189
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TCTGT) 6 BRCA2 variant considered pathogenic for breast cancer
(TCTGT;TCTGT) 0 common in clinvar
(TTCTG;TTCTG) 0 common in clinvar