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

rs12444979

From SNPedia

Orientationplus
Stabilizedplus
Make rs12444979(C;C)
Make rs12444979(C;T)
Make rs12444979(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position19922278
is asnp
is mentioned by
dbSNPrs12444979
ebirs12444979
HLIrs12444979
Exacrs12444979
Varsomers12444979
Maprs12444979
PheGenIrs12444979
hapmaprs12444979
1000 genomesrs12444979
hgdprs12444979
ensemblrs12444979
gopubmedrs12444979
geneviewrs12444979
scholarrs12444979
googlers12444979
pharmgkbrs12444979
gwascentralrs12444979
openSNPrs12444979
23andMers12444979
23andMe allrs12444979
SNP Nexus

SNPshotrs12444979
SNPdbers12444979
MSV3drs12444979
GWAS Ctlgrs12444979
GMAF0.07254
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20935630OA-icon.png]
Trait
Title Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Risk Allele C
P-val 3E-21
Odds Ratio 0.17 [0.11-0.23] kg/m2 increase

[PMID 22391884OA-icon.png] Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.


[PMID 23471855OA-icon.png] The genetics of childhood obesity and interaction with dietary macronutrients.


[PMID 27282283] UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in ukrainian females.