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rs6744682

From SNPedia

Orientationplus
Stabilizedplus
Make rs6744682(A;A)
Make rs6744682(A;T)
Make rs6744682(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position11789202
GeneLPIN1
is asnp
is mentioned by
dbSNPrs6744682
ebirs6744682
HLIrs6744682
Exacrs6744682
Varsomers6744682
Maprs6744682
PheGenIrs6744682
hapmaprs6744682
1000 genomesrs6744682
hgdprs6744682
ensemblrs6744682
gopubmedrs6744682
geneviewrs6744682
scholarrs6744682
googlers6744682
pharmgkbrs6744682
gwascentralrs6744682
openSNPrs6744682
23andMers6744682
23andMe allrs6744682
SNP Nexus

SNPshotrs6744682
SNPdbers6744682
MSV3drs6744682
GWAS Ctlgrs6744682
GMAF0.359
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 20356931] Studies of association between LPIN1 variants and common metabolic phenotypes among 17,538 Danes


[PMID 18591397OA-icon.png] Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.