rs148982608
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148982608(A;A) |
Make rs148982608(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355561 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs148982608 |
dbSNP (classic) | rs148982608 |
ClinGen | rs148982608 |
ebi | rs148982608 |
HLI | rs148982608 |
Exac | rs148982608 |
Gnomad | rs148982608 |
Varsome | rs148982608 |
LitVar | rs148982608 |
Map | rs148982608 |
PheGenI | rs148982608 |
Biobank | rs148982608 |
1000 genomes | rs148982608 |
hgdp | rs148982608 |
ensembl | rs148982608 |
geneview | rs148982608 |
scholar | rs148982608 |
rs148982608 | |
pharmgkb | rs148982608 |
gwascentral | rs148982608 |
openSNP | rs148982608 |
23andMe | rs148982608 |
SNPshot | rs148982608 |
SNPdbe | rs148982608 |
MSV3d | rs148982608 |
GWAS Ctlg | rs148982608 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148982608(A;A) |
Alt | rs148982608(A;A) |
Reference | Rs148982608(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31323338G>A |
CLNSRC | |
CLNACC |