rs137854702
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs137854702(A;G) |
Make rs137854702(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356434 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs137854702 |
dbSNP (classic) | rs137854702 |
ClinGen | rs137854702 |
ebi | rs137854702 |
HLI | rs137854702 |
Exac | rs137854702 |
Gnomad | rs137854702 |
Varsome | rs137854702 |
LitVar | rs137854702 |
Map | rs137854702 |
PheGenI | rs137854702 |
Biobank | rs137854702 |
1000 genomes | rs137854702 |
hgdp | rs137854702 |
ensembl | rs137854702 |
geneview | rs137854702 |
scholar | rs137854702 |
rs137854702 | |
pharmgkb | rs137854702 |
gwascentral | rs137854702 |
openSNP | rs137854702 |
23andMe | rs137854702 |
SNPshot | rs137854702 |
SNPdbe | rs137854702 |
MSV3d | rs137854702 |
GWAS Ctlg | rs137854702 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854702(C;C) rs137854702(G;G) rs137854702(T;T) |
Alt | rs137854702(C;C) rs137854702(G;G) rs137854702(T;T) |
Reference | Rs137854702(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324211T>A; NC_000006.11:g.31324211T>C; NC_000006.11:g.31324211T>G |
CLNSRC | |
CLNACC |