rs4713586
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs4713586(C;C) |
Make rs4713586(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32691805 |
is a | snp |
is | mentioned by |
dbSNP | rs4713586 |
dbSNP (classic) | rs4713586 |
ClinGen | rs4713586 |
ebi | rs4713586 |
HLI | rs4713586 |
Exac | rs4713586 |
Gnomad | rs4713586 |
Varsome | rs4713586 |
LitVar | rs4713586 |
Map | rs4713586 |
PheGenI | rs4713586 |
Biobank | rs4713586 |
1000 genomes | rs4713586 |
hgdp | rs4713586 |
ensembl | rs4713586 |
geneview | rs4713586 |
scholar | rs4713586 |
rs4713586 | |
pharmgkb | rs4713586 |
gwascentral | rs4713586 |
openSNP | rs4713586 |
23andMe | rs4713586 |
SNPshot | rs4713586 |
SNPdbe | rs4713586 |
MSV3d | rs4713586 |
GWAS Ctlg | rs4713586 |
GMAF | 0.07989 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs4713586 is one of three HLA region SNPs used to tag the DQ2.2 haplotype in gs221. [PMID 18509540]