rs2701175
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2701175(A;A) |
Make rs2701175(A;C) |
Make rs2701175(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 120953868 |
is a | snp |
is | mentioned by |
dbSNP | rs2701175 |
dbSNP (classic) | rs2701175 |
ClinGen | rs2701175 |
ebi | rs2701175 |
HLI | rs2701175 |
Exac | rs2701175 |
Gnomad | rs2701175 |
Varsome | rs2701175 |
LitVar | rs2701175 |
Map | rs2701175 |
PheGenI | rs2701175 |
Biobank | rs2701175 |
1000 genomes | rs2701175 |
hgdp | rs2701175 |
ensembl | rs2701175 |
geneview | rs2701175 |
scholar | rs2701175 |
rs2701175 | |
pharmgkb | rs2701175 |
gwascentral | rs2701175 |
openSNP | rs2701175 |
23andMe | rs2701175 |
SNPshot | rs2701175 |
SNPdbe | rs2701175 |
MSV3d | rs2701175 |
GWAS Ctlg | rs2701175 |
GMAF | 0.3572 |
Max Magnitude | 0 |
rs2701175 increases susceptibility to Type II Diabetes 1.33 times for carriers of the C allele [PMID 17192490]