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rs276174844(-;GTTTT)

From SNPedia
Variant of uncertain significance in ClinVar
Is agenotype
ofrs276174844
GeneBRCA2
Chromosome13
Position32,326,089
mentionedby
Magnitude1
ReputeBad
Geno Mag Summary
(-;GTTTT) 1 Variant of uncertain significance in ClinVar
(GTTTT;GTTTT) 0 common in clinvar
(TTTGT;TTTGT) 0 common in clinvar