rs72558110
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs72558110(C;T) |
Make rs72558110(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356724 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs72558110 |
dbSNP (classic) | rs72558110 |
ClinGen | rs72558110 |
ebi | rs72558110 |
HLI | rs72558110 |
Exac | rs72558110 |
Gnomad | rs72558110 |
Varsome | rs72558110 |
LitVar | rs72558110 |
Map | rs72558110 |
PheGenI | rs72558110 |
Biobank | rs72558110 |
1000 genomes | rs72558110 |
hgdp | rs72558110 |
ensembl | rs72558110 |
geneview | rs72558110 |
scholar | rs72558110 |
rs72558110 | |
pharmgkb | rs72558110 |
gwascentral | rs72558110 |
openSNP | rs72558110 |
23andMe | rs72558110 |
SNPshot | rs72558110 |
SNPdbe | rs72558110 |
MSV3d | rs72558110 |
GWAS Ctlg | rs72558110 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72558110(A;A) rs72558110(G;G) rs72558110(T;T) |
Alt | rs72558110(A;A) rs72558110(G;G) rs72558110(T;T) |
Reference | Rs72558110(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324501G>A; NC_000006.11:g.31324501G>T |
CLNSRC | |
CLNACC |