rs79493767
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs79493767(C;G) |
Make rs79493767(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943273 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs79493767 |
dbSNP (classic) | rs79493767 |
ClinGen | rs79493767 |
ebi | rs79493767 |
HLI | rs79493767 |
Exac | rs79493767 |
Gnomad | rs79493767 |
Varsome | rs79493767 |
LitVar | rs79493767 |
Map | rs79493767 |
PheGenI | rs79493767 |
Biobank | rs79493767 |
1000 genomes | rs79493767 |
hgdp | rs79493767 |
ensembl | rs79493767 |
geneview | rs79493767 |
scholar | rs79493767 |
rs79493767 | |
pharmgkb | rs79493767 |
gwascentral | rs79493767 |
openSNP | rs79493767 |
23andMe | rs79493767 |
SNPshot | rs79493767 |
SNPdbe | rs79493767 |
MSV3d | rs79493767 |
GWAS Ctlg | rs79493767 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs79493767(G;G) |
Alt | rs79493767(G;G) |
Reference | Rs79493767(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911050C>G |
CLNSRC | |
CLNACC |