rs1131279
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(C;C) | 0 | common in complete genomics |
Make rs1131279(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356181 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs1131279 |
dbSNP (classic) | rs1131279 |
ClinGen | rs1131279 |
ebi | rs1131279 |
HLI | rs1131279 |
Exac | rs1131279 |
Gnomad | rs1131279 |
Varsome | rs1131279 |
LitVar | rs1131279 |
Map | rs1131279 |
PheGenI | rs1131279 |
Biobank | rs1131279 |
1000 genomes | rs1131279 |
hgdp | rs1131279 |
ensembl | rs1131279 |
geneview | rs1131279 |
scholar | rs1131279 |
rs1131279 | |
pharmgkb | rs1131279 |
gwascentral | rs1131279 |
openSNP | rs1131279 |
23andMe | rs1131279 |
SNPshot | rs1131279 |
SNPdbe | rs1131279 |
MSV3d | rs1131279 |
GWAS Ctlg | rs1131279 |
GMAF | 0.2374 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs1131279(C;C) rs1131279(T;T) |
Alt | Rs1131279(C;C) rs1131279(T;T) |
Reference | Rs1131279(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31323958T>A; NC_000006.11:g.31323958T>G |
CLNSRC | |
CLNACC |