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rs397507886(AA;AA)
From SNPedia
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I5010392(I;I)
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common in clinvar
Is a
genotype
of
rs397507886
Gene
BRCA2
Chromosome
13
Position
32,341,171
mentioned
by
Magnitude
0
Repute
Good
Geno
Mag
Summary
(-;AA)
6
BRCA2 variant considered pathogenic for breast cancer
(AA;AA)
0
common in clinvar
Category
:
Is a genotype
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