rs1053726
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1053726(C;C) |
Make rs1053726(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31354270 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs1053726 |
dbSNP (classic) | rs1053726 |
ClinGen | rs1053726 |
ebi | rs1053726 |
HLI | rs1053726 |
Exac | rs1053726 |
Gnomad | rs1053726 |
Varsome | rs1053726 |
LitVar | rs1053726 |
Map | rs1053726 |
PheGenI | rs1053726 |
Biobank | rs1053726 |
1000 genomes | rs1053726 |
hgdp | rs1053726 |
ensembl | rs1053726 |
geneview | rs1053726 |
scholar | rs1053726 |
rs1053726 | |
pharmgkb | rs1053726 |
gwascentral | rs1053726 |
openSNP | rs1053726 |
23andMe | rs1053726 |
SNPshot | rs1053726 |
SNPdbe | rs1053726 |
MSV3d | rs1053726 |
GWAS Ctlg | rs1053726 |
GMAF | 0.1405 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1053726(A;A) rs1053726(C;C) |
Alt | rs1053726(A;A) rs1053726(C;C) |
Reference | Rs1053726(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31322047A>G |
CLNSRC | |
CLNACC |