rs887464
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs887464(A;A) |
Make rs887464(A;G) |
Make rs887464(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31178143 |
Gene | PSORS1C3 |
is a | snp |
is | mentioned by |
dbSNP | rs887464 |
dbSNP (classic) | rs887464 |
ClinGen | rs887464 |
ebi | rs887464 |
HLI | rs887464 |
Exac | rs887464 |
Gnomad | rs887464 |
Varsome | rs887464 |
LitVar | rs887464 |
Map | rs887464 |
PheGenI | rs887464 |
Biobank | rs887464 |
1000 genomes | rs887464 |
hgdp | rs887464 |
ensembl | rs887464 |
geneview | rs887464 |
scholar | rs887464 |
rs887464 | |
pharmgkb | rs887464 |
gwascentral | rs887464 |
openSNP | rs887464 |
23andMe | rs887464 |
SNPshot | rs887464 |
SNPdbe | rs887464 |
MSV3d | rs887464 |
GWAS Ctlg | rs887464 |
GMAF | 0.4004 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22837536] acute graft-versus-host disease (GVHD)
[PMID 16642438] Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene.
[PMID 18309376] Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.
[PMID 20017995] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.
[PMID 20041220] Autoimmune disease classification by inverse association with SNP alleles.