rs2308466
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2308466(A;T) |
Make rs2308466(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356226 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs2308466 |
dbSNP (classic) | rs2308466 |
ClinGen | rs2308466 |
ebi | rs2308466 |
HLI | rs2308466 |
Exac | rs2308466 |
Gnomad | rs2308466 |
Varsome | rs2308466 |
LitVar | rs2308466 |
Map | rs2308466 |
PheGenI | rs2308466 |
Biobank | rs2308466 |
1000 genomes | rs2308466 |
hgdp | rs2308466 |
ensembl | rs2308466 |
geneview | rs2308466 |
scholar | rs2308466 |
rs2308466 | |
pharmgkb | rs2308466 |
gwascentral | rs2308466 |
openSNP | rs2308466 |
23andMe | rs2308466 |
SNPshot | rs2308466 |
SNPdbe | rs2308466 |
MSV3d | rs2308466 |
GWAS Ctlg | rs2308466 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2308466(C;C) rs2308466(G;G) rs2308466(T;T) |
Alt | rs2308466(C;C) rs2308466(G;G) rs2308466(T;T) |
Reference | Rs2308466(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324003T>A; NC_000006.11:g.31324003T>C; NC_000006.11:g.31324003T>G |
CLNSRC | |
CLNACC |