Rs999737

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is asnp
is mentioned by
dbSNPrs999737
hapmaprs999737
hgdprs999737
ensemblrs999737
gopubmedrs999737
scholarrs999737
googlers999737
pharmgkbrs999737
hgvbaseg2prs999737
medrefsnprs999737
23andMers999737
SNP Nexus

GeneRAD51L1
Chromosome14
Orientationplus
Position69034682
ReferenceGRCh37 37.1/131
GenotypeEffect
rs999737(C;C)*?
rs999737(C;T)*?
rs999737(T;T)*?


? (C;C) (C;T) (T;T) 28
NIH rs999737 is located near an interesting gene, RAD51L1, which is in a pathway previously implicated in breast cancer risk. The protein encoded by this gene interacts directly with those of other genes that are involved in DNA repair and in the exchange of material between strands of DNA.

[PMID 19330030] A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

PharmGKBPA164739884
Name
AnnotationGWAS results: A multistage genome-wide association study in Breast Cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). (Initial Sample Size: 1,145 cases, 1,142 controls; Replication Sample Size: 8,625 cases, 9,657 controls); (Region: 14q24.1; Reported Gene(s): RAD51L1; Risk Allele: rs999737-C); (p-value= 0.0000002).This variant is associated with Breast Cancer.
GeneRAD51L1
Featue
EvidencePubMed ID:19330030; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesBreast Neoplasms
Curation LevelNon-Curated