rs1825630
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1825630(A;A) |
Make rs1825630(A;G) |
Make rs1825630(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 59917075 |
Gene | FHIT |
is a | snp |
is | mentioned by |
dbSNP | rs1825630 |
dbSNP (classic) | rs1825630 |
ClinGen | rs1825630 |
ebi | rs1825630 |
HLI | rs1825630 |
Exac | rs1825630 |
Gnomad | rs1825630 |
Varsome | rs1825630 |
LitVar | rs1825630 |
Map | rs1825630 |
PheGenI | rs1825630 |
Biobank | rs1825630 |
1000 genomes | rs1825630 |
hgdp | rs1825630 |
ensembl | rs1825630 |
geneview | rs1825630 |
scholar | rs1825630 |
rs1825630 | |
pharmgkb | rs1825630 |
gwascentral | rs1825630 |
openSNP | rs1825630 |
23andMe | rs1825630 |
SNPshot | rs1825630 |
SNPdbe | rs1825630 |
MSV3d | rs1825630 |
GWAS Ctlg | rs1825630 |
GMAF | 0.4642 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21223598![]() |
Trait | |
Title | Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 0.0946 [0.053-0.136] cm increase |