rs200185429
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Lower type-2 diabetes risk |
Make rs200185429(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 8 |
Position | 117153084 |
Gene | LOC105375716, SLC30A8 |
is a | snp |
is | mentioned by |
dbSNP | rs200185429 |
dbSNP (classic) | rs200185429 |
ClinGen | rs200185429 |
ebi | rs200185429 |
HLI | rs200185429 |
Exac | rs200185429 |
Gnomad | rs200185429 |
Varsome | rs200185429 |
LitVar | rs200185429 |
Map | rs200185429 |
PheGenI | rs200185429 |
Biobank | rs200185429 |
1000 genomes | rs200185429 |
hgdp | rs200185429 |
ensembl | rs200185429 |
geneview | rs200185429 |
scholar | rs200185429 |
rs200185429 | |
pharmgkb | rs200185429 |
gwascentral | rs200185429 |
openSNP | rs200185429 |
23andMe | rs200185429 |
SNPshot | rs200185429 |
SNPdbe | rs200185429 |
MSV3d | rs200185429 |
GWAS Ctlg | rs200185429 |
Max Magnitude | 3 |
rs200185429, also known as c.412C>T, p.Arg138Ter and R138X, is perhaps the best studied of over 10 loss-of-function variants found in the SLC30A8 gene to reduce risk of developing type-2 diabetes by about 2/3rds (OR:0.34, p=1.7×10e−6) in a large Icelandic study published in 2014.[PMID 24584071]