rs137854696
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137854696(C;C) |
Make rs137854696(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356688 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs137854696 |
dbSNP (classic) | rs137854696 |
ClinGen | rs137854696 |
ebi | rs137854696 |
HLI | rs137854696 |
Exac | rs137854696 |
Gnomad | rs137854696 |
Varsome | rs137854696 |
LitVar | rs137854696 |
Map | rs137854696 |
PheGenI | rs137854696 |
Biobank | rs137854696 |
1000 genomes | rs137854696 |
hgdp | rs137854696 |
ensembl | rs137854696 |
geneview | rs137854696 |
scholar | rs137854696 |
rs137854696 | |
pharmgkb | rs137854696 |
gwascentral | rs137854696 |
openSNP | rs137854696 |
23andMe | rs137854696 |
SNPshot | rs137854696 |
SNPdbe | rs137854696 |
MSV3d | rs137854696 |
GWAS Ctlg | rs137854696 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854696(A;A) rs137854696(C;C) rs137854696(T;T) |
Alt | rs137854696(A;A) rs137854696(C;C) rs137854696(T;T) |
Reference | Rs137854696(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324465C>A; NC_000006.11:g.31324465C>G; NC_000006.11:g.31324465C>T |
CLNSRC | |
CLNACC |