rs1206634
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1206634(A;A) |
Make rs1206634(A;C) |
Make rs1206634(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 96302380 |
is a | snp |
is | mentioned by |
dbSNP | rs1206634 |
dbSNP (classic) | rs1206634 |
ClinGen | rs1206634 |
ebi | rs1206634 |
HLI | rs1206634 |
Exac | rs1206634 |
Gnomad | rs1206634 |
Varsome | rs1206634 |
LitVar | rs1206634 |
Map | rs1206634 |
PheGenI | rs1206634 |
Biobank | rs1206634 |
1000 genomes | rs1206634 |
hgdp | rs1206634 |
ensembl | rs1206634 |
geneview | rs1206634 |
scholar | rs1206634 |
rs1206634 | |
pharmgkb | rs1206634 |
gwascentral | rs1206634 |
openSNP | rs1206634 |
23andMe | rs1206634 |
SNPshot | rs1206634 |
SNPdbe | rs1206634 |
MSV3d | rs1206634 |
GWAS Ctlg | rs1206634 |
GMAF | 0.0532 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23869418] Association Between a 11β-Hydroxysteroid Dehydrogenase Type 1 Gene Polymorphism and Metabolic Syndrome in a South Indian Population