rs1059467
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1059467(G;G) |
Make rs1059467(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942966 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs1059467 |
dbSNP (classic) | rs1059467 |
ClinGen | rs1059467 |
ebi | rs1059467 |
HLI | rs1059467 |
Exac | rs1059467 |
Gnomad | rs1059467 |
Varsome | rs1059467 |
LitVar | rs1059467 |
Map | rs1059467 |
PheGenI | rs1059467 |
Biobank | rs1059467 |
1000 genomes | rs1059467 |
hgdp | rs1059467 |
ensembl | rs1059467 |
geneview | rs1059467 |
scholar | rs1059467 |
rs1059467 | |
pharmgkb | rs1059467 |
gwascentral | rs1059467 |
openSNP | rs1059467 |
23andMe | rs1059467 |
SNPshot | rs1059467 |
SNPdbe | rs1059467 |
MSV3d | rs1059467 |
GWAS Ctlg | rs1059467 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1059467(A;A) rs1059467(C;C) rs1059467(G;G) |
Alt | rs1059467(A;A) rs1059467(C;C) rs1059467(G;G) |
Reference | Rs1059467(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910743T>A; NC_000006.11:g.29910743T>C; NC_000006.11:g.29910743T>G |
CLNSRC | |
CLNACC |