rs281864767
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs281864767(A;A) |
Make rs281864767(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29944208 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs281864767 |
dbSNP (classic) | rs281864767 |
ClinGen | rs281864767 |
ebi | rs281864767 |
HLI | rs281864767 |
Exac | rs281864767 |
Gnomad | rs281864767 |
Varsome | rs281864767 |
LitVar | rs281864767 |
Map | rs281864767 |
PheGenI | rs281864767 |
Biobank | rs281864767 |
1000 genomes | rs281864767 |
hgdp | rs281864767 |
ensembl | rs281864767 |
geneview | rs281864767 |
scholar | rs281864767 |
rs281864767 | |
pharmgkb | rs281864767 |
gwascentral | rs281864767 |
openSNP | rs281864767 |
23andMe | rs281864767 |
SNPshot | rs281864767 |
SNPdbe | rs281864767 |
MSV3d | rs281864767 |
GWAS Ctlg | rs281864767 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs281864767(A;A) |
Alt | rs281864767(A;A) |
Reference | Rs281864767(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911985G>A |
CLNSRC | |
CLNACC |