rs151341249
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs151341249(A;T) |
Make rs151341249(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356314 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs151341249 |
dbSNP (classic) | rs151341249 |
ClinGen | rs151341249 |
ebi | rs151341249 |
HLI | rs151341249 |
Exac | rs151341249 |
Gnomad | rs151341249 |
Varsome | rs151341249 |
LitVar | rs151341249 |
Map | rs151341249 |
PheGenI | rs151341249 |
Biobank | rs151341249 |
1000 genomes | rs151341249 |
hgdp | rs151341249 |
ensembl | rs151341249 |
geneview | rs151341249 |
scholar | rs151341249 |
rs151341249 | |
pharmgkb | rs151341249 |
gwascentral | rs151341249 |
openSNP | rs151341249 |
23andMe | rs151341249 |
SNPshot | rs151341249 |
SNPdbe | rs151341249 |
MSV3d | rs151341249 |
GWAS Ctlg | rs151341249 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151341249(T;T) |
Alt | rs151341249(T;T) |
Reference | Rs151341249(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324091T>A |
CLNSRC | |
CLNACC |