rs3177891
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3177891(C;T) |
Make rs3177891(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356914 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs3177891 |
dbSNP (classic) | rs3177891 |
ClinGen | rs3177891 |
ebi | rs3177891 |
HLI | rs3177891 |
Exac | rs3177891 |
Gnomad | rs3177891 |
Varsome | rs3177891 |
LitVar | rs3177891 |
Map | rs3177891 |
PheGenI | rs3177891 |
Biobank | rs3177891 |
1000 genomes | rs3177891 |
hgdp | rs3177891 |
ensembl | rs3177891 |
geneview | rs3177891 |
scholar | rs3177891 |
rs3177891 | |
pharmgkb | rs3177891 |
gwascentral | rs3177891 |
openSNP | rs3177891 |
23andMe | rs3177891 |
SNPshot | rs3177891 |
SNPdbe | rs3177891 |
MSV3d | rs3177891 |
GWAS Ctlg | rs3177891 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs3177891(G;G) rs3177891(T;T) |
Alt | rs3177891(G;G) rs3177891(T;T) |
Reference | Rs3177891(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324691G>A; NC_000006.11:g.31324691G>C |
CLNSRC | |
CLNACC |