rs1071592
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1071592(A;A) |
Make rs1071592(A;C) |
Make rs1071592(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 186620636 |
Gene | AHSG |
is a | snp |
is | mentioned by |
dbSNP | rs1071592 |
dbSNP (classic) | rs1071592 |
ClinGen | rs1071592 |
ebi | rs1071592 |
HLI | rs1071592 |
Exac | rs1071592 |
Gnomad | rs1071592 |
Varsome | rs1071592 |
LitVar | rs1071592 |
Map | rs1071592 |
PheGenI | rs1071592 |
Biobank | rs1071592 |
1000 genomes | rs1071592 |
hgdp | rs1071592 |
ensembl | rs1071592 |
geneview | rs1071592 |
scholar | rs1071592 |
rs1071592 | |
pharmgkb | rs1071592 |
gwascentral | rs1071592 |
openSNP | rs1071592 |
23andMe | rs1071592 |
SNPshot | rs1071592 |
SNPdbe | rs1071592 |
MSV3d | rs1071592 |
GWAS Ctlg | rs1071592 |
GMAF | 0.2121 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19358088] AHSG Gene Variation is not Associated with Regional Body Fat Distribution - A Magnetic Resonance Study.
[PMID 16046317] A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.
[PMID 19098027] SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.