rs9266162
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs9266162(C;C) |
Make rs9266162(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356718 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs9266162 |
dbSNP (classic) | rs9266162 |
ClinGen | rs9266162 |
ebi | rs9266162 |
HLI | rs9266162 |
Exac | rs9266162 |
Gnomad | rs9266162 |
Varsome | rs9266162 |
LitVar | rs9266162 |
Map | rs9266162 |
PheGenI | rs9266162 |
Biobank | rs9266162 |
1000 genomes | rs9266162 |
hgdp | rs9266162 |
ensembl | rs9266162 |
geneview | rs9266162 |
scholar | rs9266162 |
rs9266162 | |
pharmgkb | rs9266162 |
gwascentral | rs9266162 |
openSNP | rs9266162 |
23andMe | rs9266162 |
SNPshot | rs9266162 |
SNPdbe | rs9266162 |
MSV3d | rs9266162 |
GWAS Ctlg | rs9266162 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs9266162(A;A) rs9266162(C;C) rs9266162(T;T) |
Alt | rs9266162(A;A) rs9266162(C;C) rs9266162(T;T) |
Reference | Rs9266162(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31324495G>A; NC_000006.11:g.31324495G>C; NC_000006.11:g.31324495G>T |
CLNSRC | |
CLNACC |