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rs11695610

From SNPedia

Orientationplus
Stabilizedplus
Make rs11695610(C;C)
Make rs11695610(C;G)
Make rs11695610(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position11796465
GeneLPIN1
is asnp
is mentioned by
dbSNPrs11695610
ebirs11695610
HLIrs11695610
Exacrs11695610
Varsomers11695610
Maprs11695610
PheGenIrs11695610
hapmaprs11695610
1000 genomesrs11695610
hgdprs11695610
ensemblrs11695610
gopubmedrs11695610
geneviewrs11695610
scholarrs11695610
googlers11695610
pharmgkbrs11695610
gwascentralrs11695610
openSNPrs11695610
23andMers11695610
23andMe allrs11695610
SNP Nexus

SNPshotrs11695610
SNPdbers11695610
MSV3drs11695610
GWAS Ctlgrs11695610
GMAF0.09504
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22853689] Genetic variants of LPIN1 indicate an association with Type 2 diabetes mellitus in a Chinese population