rs1169310
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1169310(A;A) |
Make rs1169310(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 121001630 |
Gene | HNF1A |
is a | snp |
is | mentioned by |
dbSNP | rs1169310 |
dbSNP (classic) | rs1169310 |
ClinGen | rs1169310 |
ebi | rs1169310 |
HLI | rs1169310 |
Exac | rs1169310 |
Gnomad | rs1169310 |
Varsome | rs1169310 |
LitVar | rs1169310 |
Map | rs1169310 |
PheGenI | rs1169310 |
Biobank | rs1169310 |
1000 genomes | rs1169310 |
hgdp | rs1169310 |
ensembl | rs1169310 |
geneview | rs1169310 |
scholar | rs1169310 |
rs1169310 | |
pharmgkb | rs1169310 |
gwascentral | rs1169310 |
openSNP | rs1169310 |
23andMe | rs1169310 |
SNPshot | rs1169310 |
SNPdbe | rs1169310 |
MSV3d | rs1169310 |
GWAS Ctlg | rs1169310 |
GMAF | 0.3669 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs1169310 |
PubMedID | [PMID 18439552] |
Condition | C-reactive protein |
Gene | HNF1A |
Risk Allele | A |
pValue | 2.00E-008 |
OR | 0.13 |
95% CI | 0.08-0.17) mg/l decrease in log(CRP) leve |
[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
[PMID 21195701] Effect of obesity on the association between common variations in the HNF1A gene region and C-reactive protein level in Taiwanese.
ClinVar | |
---|---|
Risk | rs1169310(A;A) |
Alt | rs1169310(A;A) |
Reference | Rs1169310(G;G) |
Significance | Non-pathogenic |
Disease | Maturity-onset diabetes of the young |
Variation | info |
Gene | HNF1A |
CLNDBN | Maturity-onset diabetes of the young |
Reversed | 0 |
HGVS | NC_000012.11:g.121439433G>A |
CLNSRC | |
CLNACC | RCV000402135.1, |