rs11695610
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11695610(C;C) |
Make rs11695610(C;G) |
Make rs11695610(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 11796465 |
Gene | LPIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs11695610 |
dbSNP (classic) | rs11695610 |
ClinGen | rs11695610 |
ebi | rs11695610 |
HLI | rs11695610 |
Exac | rs11695610 |
Gnomad | rs11695610 |
Varsome | rs11695610 |
LitVar | rs11695610 |
Map | rs11695610 |
PheGenI | rs11695610 |
Biobank | rs11695610 |
1000 genomes | rs11695610 |
hgdp | rs11695610 |
ensembl | rs11695610 |
geneview | rs11695610 |
scholar | rs11695610 |
rs11695610 | |
pharmgkb | rs11695610 |
gwascentral | rs11695610 |
openSNP | rs11695610 |
23andMe | rs11695610 |
SNPshot | rs11695610 |
SNPdbe | rs11695610 |
MSV3d | rs11695610 |
GWAS Ctlg | rs11695610 |
GMAF | 0.09504 |
Max Magnitude | 0 |
? | (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