rs4671386
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4671386(A;A) |
Make rs4671386(A;C) |
Make rs4671386(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 60287858 |
is a | snp |
is | mentioned by |
dbSNP | rs4671386 |
dbSNP (classic) | rs4671386 |
ClinGen | rs4671386 |
ebi | rs4671386 |
HLI | rs4671386 |
Exac | rs4671386 |
Gnomad | rs4671386 |
Varsome | rs4671386 |
LitVar | rs4671386 |
Map | rs4671386 |
PheGenI | rs4671386 |
Biobank | rs4671386 |
1000 genomes | rs4671386 |
hgdp | rs4671386 |
ensembl | rs4671386 |
geneview | rs4671386 |
scholar | rs4671386 |
rs4671386 | |
pharmgkb | rs4671386 |
gwascentral | rs4671386 |
openSNP | rs4671386 |
23andMe | rs4671386 |
SNPshot | rs4671386 |
SNPdbe | rs4671386 |
MSV3d | rs4671386 |
GWAS Ctlg | rs4671386 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24927181] |
Trait | Acne (severe) |
Title | Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. |
Risk Allele | C |
P-val | 2E-6 |
Odds Ratio | 1.19 [1.11-1.3] |