Rs766173

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is asnp
is mentioned by
dbSNPrs766173
hapmaprs766173
hgdprs766173
ensemblrs766173
gopubmedrs766173
scholarrs766173
googlers766173
pharmgkbrs766173
hgvbaseg2prs766173
medrefsnprs766173
23andMers766173
SNP Nexus

GeneBRCA2
Chromosome13
Orientationminus
Position31804480
GenotypeEffect
rs766173(G;G)
rs766173(G;T)*?
rs766173(T;T)


Genotypes Magnitude Summary
Rs766173(G;G) 22
Rs766173(T;T) 00
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
? (G;T) (T;T)