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rs397507890(TTTCGG;TTTCGG)

From SNPedia
common in clinvar
Is agenotype
ofrs397507890
GeneBRCA2
Chromosome13
Position32,346,893
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TTCGGT) 6 BRCA2 variant considered pathogenic for breast cancer
(TTCGGT;TTCGGT) 0 common in clinvar
(TTTCGG;TTTCGG) 0 common in clinvar