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rs1079866

From SNPedia

Orientationminus
Stabilizedminus
Make rs1079866(C;C)
Make rs1079866(C;G)
Make rs1079866(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position41430495
is asnp
is mentioned by
dbSNPrs1079866
ebirs1079866
HLIrs1079866
Exacrs1079866
Varsomers1079866
Maprs1079866
PheGenIrs1079866
hapmaprs1079866
1000 genomesrs1079866
hgdprs1079866
ensemblrs1079866
gopubmedrs1079866
geneviewrs1079866
scholarrs1079866
googlers1079866
pharmgkbrs1079866
gwascentralrs1079866
openSNPrs1079866
23andMers1079866
23andMe allrs1079866
SNP Nexus

SNPshotrs1079866
SNPdbers1079866
MSV3drs1079866
GWAS Ctlgrs1079866
GMAF0.135
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21102462OA-icon.png]
Trait
Title Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Risk Allele G
P-val 6E-14
Odds Ratio 3.9000 [2.92-4.88] week increase


[PMID 22433456OA-icon.png] Reproductive aging associated common genetic variants and the risk of breast cancer