rs151341372
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs151341372(C;T) |
Make rs151341372(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355333 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs151341372 |
dbSNP (classic) | rs151341372 |
ClinGen | rs151341372 |
ebi | rs151341372 |
HLI | rs151341372 |
Exac | rs151341372 |
Gnomad | rs151341372 |
Varsome | rs151341372 |
LitVar | rs151341372 |
Map | rs151341372 |
PheGenI | rs151341372 |
Biobank | rs151341372 |
1000 genomes | rs151341372 |
hgdp | rs151341372 |
ensembl | rs151341372 |
geneview | rs151341372 |
scholar | rs151341372 |
rs151341372 | |
pharmgkb | rs151341372 |
gwascentral | rs151341372 |
openSNP | rs151341372 |
23andMe | rs151341372 |
SNPshot | rs151341372 |
SNPdbe | rs151341372 |
MSV3d | rs151341372 |
GWAS Ctlg | rs151341372 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151341372(T;T) |
Alt | rs151341372(T;T) |
Reference | Rs151341372(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31323110G>A |
CLNSRC | |
CLNACC |