rs1064588
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1064588(A;G) |
Make rs1064588(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942940 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs1064588 |
dbSNP (classic) | rs1064588 |
ClinGen | rs1064588 |
ebi | rs1064588 |
HLI | rs1064588 |
Exac | rs1064588 |
Gnomad | rs1064588 |
Varsome | rs1064588 |
LitVar | rs1064588 |
Map | rs1064588 |
PheGenI | rs1064588 |
Biobank | rs1064588 |
1000 genomes | rs1064588 |
hgdp | rs1064588 |
ensembl | rs1064588 |
geneview | rs1064588 |
scholar | rs1064588 |
rs1064588 | |
pharmgkb | rs1064588 |
gwascentral | rs1064588 |
openSNP | rs1064588 |
23andMe | rs1064588 |
SNPshot | rs1064588 |
SNPdbe | rs1064588 |
MSV3d | rs1064588 |
GWAS Ctlg | rs1064588 |
GMAF | 0.04775 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064588(C;C) rs1064588(G;G) rs1064588(T;T) |
Alt | rs1064588(C;C) rs1064588(G;G) rs1064588(T;T) |
Reference | Rs1064588(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910717A>C; NC_000006.11:g.29910717A>G; NC_000006.11:g.29910717A>T |
CLNSRC | |
CLNACC |