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rs146052672

From SNPedia

Merged intors139876191
Orientationplus
Stabilizedplus
Make rs146052672(-;-)
Make rs146052672(-;C)
Make rs146052672(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position34242693
GeneHMGA1
is asnp
is mentioned by
dbSNPrs146052672
ebirs146052672
HLIrs146052672
Exacrs146052672
Varsomers146052672
Maprs146052672
PheGenIrs146052672
hapmaprs146052672
1000 genomesrs146052672
hgdprs146052672
ensemblrs146052672
gopubmedrs146052672
geneviewrs146052672
scholarrs146052672
googlers146052672
pharmgkbrs146052672
gwascentralrs146052672
openSNPrs146052672
23andMers146052672
23andMe allrs146052672
SNP Nexus

SNPshotrs146052672
SNPdbers146052672
MSV3drs146052672
GWAS Ctlgrs146052672
StatusMerged into rs139876191
Max Magnitude

[PMID 23512162OA-icon.png] A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components

[PMID 24148075] Evidence that an HMGA1 Gene Variant Associates with Type 2 Diabetes, Body Mass Index, and High-Density Lipoprotein Cholesterol in a Hispanic-American Population

[PMID 26296198OA-icon.png] The Association between HMGA1 rs146052672 Variant and Type 2 Diabetes: A Transethnic Meta-Analysis