Rs766173

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is asnp
is mentioned by
dbSNPrs766173
nextbiors766173
hapmaprs766173
1000 genomesrs766173
hgdprs766173
ensemblrs766173
gopubmedrs766173
scholarrs766173
googlers766173
pharmgkbrs766173
gwascentralrs766173
openSNPrs766173
23andMers766173
23andMe allrs766173
SNP Nexus

SNPshotrs766173
SNPdbers766173
MSV3drs766173
GeneBRCA2
Chromosome13
Orientationminus
Position32906480
ReferenceGRCh37 37.1/131
Max Magnitude2
Geno Mag Summary
(G;G) 2
(T;T) 0
Make rs766173(G;T)
? (G;G) (G;T) (T;T) 28
This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, but cumulatively significant, increased risk for breast cancer. [PMID 17341484]

For details of all 25 SNPs in this group, along with the two methods used to calculate overall risk estimates for breast cancer, refer to the SNPedia breast cancer entry.

For this particular SNP, the risk (minor) allele is (G).

Neighborrs144848
Distance249
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