rs45585732
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45585732(A;A) |
Make rs45585732(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942772 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs45585732 |
dbSNP (classic) | rs45585732 |
ClinGen | rs45585732 |
ebi | rs45585732 |
HLI | rs45585732 |
Exac | rs45585732 |
Gnomad | rs45585732 |
Varsome | rs45585732 |
LitVar | rs45585732 |
Map | rs45585732 |
PheGenI | rs45585732 |
Biobank | rs45585732 |
1000 genomes | rs45585732 |
hgdp | rs45585732 |
ensembl | rs45585732 |
geneview | rs45585732 |
scholar | rs45585732 |
rs45585732 | |
pharmgkb | rs45585732 |
gwascentral | rs45585732 |
openSNP | rs45585732 |
23andMe | rs45585732 |
SNPshot | rs45585732 |
SNPdbe | rs45585732 |
MSV3d | rs45585732 |
GWAS Ctlg | rs45585732 |
GMAF | 0.02801 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45585732(A;A) |
Alt | rs45585732(A;A) |
Reference | Rs45585732(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910549G>A |
CLNSRC | |
CLNACC |