rs45482492
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45482492(A;A) |
Make rs45482492(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943378 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs45482492 |
dbSNP (classic) | rs45482492 |
ClinGen | rs45482492 |
ebi | rs45482492 |
HLI | rs45482492 |
Exac | rs45482492 |
Gnomad | rs45482492 |
Varsome | rs45482492 |
LitVar | rs45482492 |
Map | rs45482492 |
PheGenI | rs45482492 |
Biobank | rs45482492 |
1000 genomes | rs45482492 |
hgdp | rs45482492 |
ensembl | rs45482492 |
geneview | rs45482492 |
scholar | rs45482492 |
rs45482492 | |
pharmgkb | rs45482492 |
gwascentral | rs45482492 |
openSNP | rs45482492 |
23andMe | rs45482492 |
SNPshot | rs45482492 |
SNPdbe | rs45482492 |
MSV3d | rs45482492 |
GWAS Ctlg | rs45482492 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45482492(A;A) rs45482492(C;C) rs45482492(T;T) |
Alt | rs45482492(A;A) rs45482492(C;C) rs45482492(T;T) |
Reference | Rs45482492(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911155G>A; NC_000006.11:g.29911155G>C; NC_000006.11:g.29911155G>T |
CLNSRC | |
CLNACC |