rs147947139
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs147947139(A;A) |
Make rs147947139(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29945161 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs147947139 |
dbSNP (classic) | rs147947139 |
ClinGen | rs147947139 |
ebi | rs147947139 |
HLI | rs147947139 |
Exac | rs147947139 |
Gnomad | rs147947139 |
Varsome | rs147947139 |
LitVar | rs147947139 |
Map | rs147947139 |
PheGenI | rs147947139 |
Biobank | rs147947139 |
1000 genomes | rs147947139 |
hgdp | rs147947139 |
ensembl | rs147947139 |
geneview | rs147947139 |
scholar | rs147947139 |
rs147947139 | |
pharmgkb | rs147947139 |
gwascentral | rs147947139 |
openSNP | rs147947139 |
23andMe | rs147947139 |
SNPshot | rs147947139 |
SNPdbe | rs147947139 |
MSV3d | rs147947139 |
GWAS Ctlg | rs147947139 |
GMAF | 0.1529 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147947139(A;A) |
Alt | rs147947139(A;A) |
Reference | Rs147947139(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29912938C>A |
CLNSRC | |
CLNACC |