Have questions? Visit https://www.reddit.com/r/SNPedia

rs4987945

From SNPedia

Merged intors2227924
Orientationplus
Stabilizedplus
Make rs4987945(C;C)
Make rs4987945(C;G)
Make rs4987945(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position108251865
GeneATM
is asnp
is mentioned by
dbSNPrs4987945
ebirs4987945
HLIrs4987945
Exacrs4987945
Varsomers4987945
Maprs4987945
PheGenIrs4987945
hapmaprs4987945
1000 genomesrs4987945
hgdprs4987945
ensemblrs4987945
gopubmedrs4987945
geneviewrs4987945
scholarrs4987945
googlers4987945
pharmgkbrs4987945
gwascentralrs4987945
openSNPrs4987945
23andMers4987945
23andMe allrs4987945
SNP Nexus

SNPshotrs4987945
SNPdbers4987945
MSV3drs4987945
GWAS Ctlgrs4987945
StatusMerged into rs2227924
Max Magnitude
? (C;C) (C;G) (G;G) 28
This SNP, a variant in the ATM 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).