rs111301312
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs111301312(G;G) |
Make rs111301312(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31354331 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs111301312 |
dbSNP (classic) | rs111301312 |
ClinGen | rs111301312 |
ebi | rs111301312 |
HLI | rs111301312 |
Exac | rs111301312 |
Gnomad | rs111301312 |
Varsome | rs111301312 |
LitVar | rs111301312 |
Map | rs111301312 |
PheGenI | rs111301312 |
Biobank | rs111301312 |
1000 genomes | rs111301312 |
hgdp | rs111301312 |
ensembl | rs111301312 |
geneview | rs111301312 |
scholar | rs111301312 |
rs111301312 | |
pharmgkb | rs111301312 |
gwascentral | rs111301312 |
openSNP | rs111301312 |
23andMe | rs111301312 |
SNPshot | rs111301312 |
SNPdbe | rs111301312 |
MSV3d | rs111301312 |
GWAS Ctlg | rs111301312 |
GMAF | 0.04224 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs111301312(G;G) rs111301312(C;C) |
Alt | rs111301312(G;G) rs111301312(C;C) |
Reference | Rs111301312(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31322108T>G |
CLNSRC | |
CLNACC |