rs79051037
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs79051037(A;A) |
Make rs79051037(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356918 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs79051037 |
dbSNP (classic) | rs79051037 |
ClinGen | rs79051037 |
ebi | rs79051037 |
HLI | rs79051037 |
Exac | rs79051037 |
Gnomad | rs79051037 |
Varsome | rs79051037 |
LitVar | rs79051037 |
Map | rs79051037 |
PheGenI | rs79051037 |
Biobank | rs79051037 |
1000 genomes | rs79051037 |
hgdp | rs79051037 |
ensembl | rs79051037 |
geneview | rs79051037 |
scholar | rs79051037 |
rs79051037 | |
pharmgkb | rs79051037 |
gwascentral | rs79051037 |
openSNP | rs79051037 |
23andMe | rs79051037 |
SNPshot | rs79051037 |
SNPdbe | rs79051037 |
MSV3d | rs79051037 |
GWAS Ctlg | rs79051037 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs79051037(A;A) |
Alt | rs79051037(A;A) |
Reference | Rs79051037(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324695C>T |
CLNSRC | |
CLNACC |