rs45560938
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs45560938(G;G) |
Make rs45560938(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31357084 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs45560938 |
dbSNP (classic) | rs45560938 |
ClinGen | rs45560938 |
ebi | rs45560938 |
HLI | rs45560938 |
Exac | rs45560938 |
Gnomad | rs45560938 |
Varsome | rs45560938 |
LitVar | rs45560938 |
Map | rs45560938 |
PheGenI | rs45560938 |
Biobank | rs45560938 |
1000 genomes | rs45560938 |
hgdp | rs45560938 |
ensembl | rs45560938 |
geneview | rs45560938 |
scholar | rs45560938 |
rs45560938 | |
pharmgkb | rs45560938 |
gwascentral | rs45560938 |
openSNP | rs45560938 |
23andMe | rs45560938 |
SNPshot | rs45560938 |
SNPdbe | rs45560938 |
MSV3d | rs45560938 |
GWAS Ctlg | rs45560938 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45560938(G;G) |
Alt | rs45560938(G;G) |
Reference | Rs45560938(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324861A>C |
CLNSRC | |
CLNACC |