rs45474295
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs45474295(A;C) |
Make rs45474295(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943408 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs45474295 |
dbSNP (classic) | rs45474295 |
ClinGen | rs45474295 |
ebi | rs45474295 |
HLI | rs45474295 |
Exac | rs45474295 |
Gnomad | rs45474295 |
Varsome | rs45474295 |
LitVar | rs45474295 |
Map | rs45474295 |
PheGenI | rs45474295 |
Biobank | rs45474295 |
1000 genomes | rs45474295 |
hgdp | rs45474295 |
ensembl | rs45474295 |
geneview | rs45474295 |
scholar | rs45474295 |
rs45474295 | |
pharmgkb | rs45474295 |
gwascentral | rs45474295 |
openSNP | rs45474295 |
23andMe | rs45474295 |
SNPshot | rs45474295 |
SNPdbe | rs45474295 |
MSV3d | rs45474295 |
GWAS Ctlg | rs45474295 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45474295(C;C) rs45474295(G;G) rs45474295(T;T) |
Alt | rs45474295(C;C) rs45474295(G;G) rs45474295(T;T) |
Reference | Rs45474295(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911185A>C; NC_000006.11:g.29911185A>G; NC_000006.11:g.29911185A>T |
CLNSRC | |
CLNACC |