rs145974360
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs145974360(C;C) |
Make rs145974360(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356805 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs145974360 |
dbSNP (classic) | rs145974360 |
ClinGen | rs145974360 |
ebi | rs145974360 |
HLI | rs145974360 |
Exac | rs145974360 |
Gnomad | rs145974360 |
Varsome | rs145974360 |
LitVar | rs145974360 |
Map | rs145974360 |
PheGenI | rs145974360 |
Biobank | rs145974360 |
1000 genomes | rs145974360 |
hgdp | rs145974360 |
ensembl | rs145974360 |
geneview | rs145974360 |
scholar | rs145974360 |
rs145974360 | |
pharmgkb | rs145974360 |
gwascentral | rs145974360 |
openSNP | rs145974360 |
23andMe | rs145974360 |
SNPshot | rs145974360 |
SNPdbe | rs145974360 |
MSV3d | rs145974360 |
GWAS Ctlg | rs145974360 |
GMAF | 0.01056 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs145974360(C;C) |
Alt | rs145974360(C;C) |
Reference | Rs145974360(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31324582T>C |
CLNSRC | |
CLNACC |