rs2596492
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs2596492(C;C) |
Make rs2596492(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356934 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs2596492 |
dbSNP (classic) | rs2596492 |
ClinGen | rs2596492 |
ebi | rs2596492 |
HLI | rs2596492 |
Exac | rs2596492 |
Gnomad | rs2596492 |
Varsome | rs2596492 |
LitVar | rs2596492 |
Map | rs2596492 |
PheGenI | rs2596492 |
Biobank | rs2596492 |
1000 genomes | rs2596492 |
hgdp | rs2596492 |
ensembl | rs2596492 |
geneview | rs2596492 |
scholar | rs2596492 |
rs2596492 | |
pharmgkb | rs2596492 |
gwascentral | rs2596492 |
openSNP | rs2596492 |
23andMe | rs2596492 |
SNPshot | rs2596492 |
SNPdbe | rs2596492 |
MSV3d | rs2596492 |
GWAS Ctlg | rs2596492 |
GMAF | 0.1635 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2596492(C;C) rs2596492(G;G) |
Alt | rs2596492(C;C) rs2596492(G;G) |
Reference | Rs2596492(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324711A>C; NC_000006.11:g.31324711A>G |
CLNSRC | |
CLNACC |