rs1059451
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1059451(A;A) |
Make rs1059451(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942922 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs1059451 |
dbSNP (classic) | rs1059451 |
ClinGen | rs1059451 |
ebi | rs1059451 |
HLI | rs1059451 |
Exac | rs1059451 |
Gnomad | rs1059451 |
Varsome | rs1059451 |
LitVar | rs1059451 |
Map | rs1059451 |
PheGenI | rs1059451 |
Biobank | rs1059451 |
1000 genomes | rs1059451 |
hgdp | rs1059451 |
ensembl | rs1059451 |
geneview | rs1059451 |
scholar | rs1059451 |
rs1059451 | |
pharmgkb | rs1059451 |
gwascentral | rs1059451 |
openSNP | rs1059451 |
23andMe | rs1059451 |
SNPshot | rs1059451 |
SNPdbe | rs1059451 |
MSV3d | rs1059451 |
GWAS Ctlg | rs1059451 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1059451(A;A) |
Alt | rs1059451(A;A) |
Reference | Rs1059451(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910699G>A |
CLNSRC | |
CLNACC |