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rs16882214

From SNPedia

Orientationplus
Stabilizedplus
Make rs16882214(C;C)
Make rs16882214(C;G)
Make rs16882214(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position19443704
is asnp
is mentioned by
dbSNPrs16882214
ebirs16882214
HLIrs16882214
Exacrs16882214
Varsomers16882214
Maprs16882214
PheGenIrs16882214
hapmaprs16882214
1000 genomesrs16882214
hgdprs16882214
ensemblrs16882214
gopubmedrs16882214
geneviewrs16882214
scholarrs16882214
googlers16882214
pharmgkbrs16882214
gwascentralrs16882214
openSNPrs16882214
23andMers16882214
23andMe allrs16882214
SNP Nexus

SNPshotrs16882214
SNPdbers16882214
MSV3drs16882214
GWAS Ctlgrs16882214
GMAF0.1198
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23354978OA-icon.png]
Trait Breast cancer
Title Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.
Risk Allele
P-val 2E-6
Odds Ratio 1.43 [NR]