rs11539959
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11539959(C;C) |
Make rs11539959(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942864 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs11539959 |
dbSNP (classic) | rs11539959 |
ClinGen | rs11539959 |
ebi | rs11539959 |
HLI | rs11539959 |
Exac | rs11539959 |
Gnomad | rs11539959 |
Varsome | rs11539959 |
LitVar | rs11539959 |
Map | rs11539959 |
PheGenI | rs11539959 |
Biobank | rs11539959 |
1000 genomes | rs11539959 |
hgdp | rs11539959 |
ensembl | rs11539959 |
geneview | rs11539959 |
scholar | rs11539959 |
rs11539959 | |
pharmgkb | rs11539959 |
gwascentral | rs11539959 |
openSNP | rs11539959 |
23andMe | rs11539959 |
SNPshot | rs11539959 |
SNPdbe | rs11539959 |
MSV3d | rs11539959 |
GWAS Ctlg | rs11539959 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11539959(A;A) rs11539959(C;C) rs11539959(T;T) |
Alt | rs11539959(A;A) rs11539959(C;C) rs11539959(T;T) |
Reference | Rs11539959(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910641G>A; NC_000006.11:g.29910641G>C; NC_000006.11:g.29910641G>T |
CLNSRC | |
CLNACC |