rs709052
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs709052(C;C) |
Make rs709052(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355456 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs709052 |
dbSNP (classic) | rs709052 |
ClinGen | rs709052 |
ebi | rs709052 |
HLI | rs709052 |
Exac | rs709052 |
Gnomad | rs709052 |
Varsome | rs709052 |
LitVar | rs709052 |
Map | rs709052 |
PheGenI | rs709052 |
Biobank | rs709052 |
1000 genomes | rs709052 |
hgdp | rs709052 |
ensembl | rs709052 |
geneview | rs709052 |
scholar | rs709052 |
rs709052 | |
pharmgkb | rs709052 |
gwascentral | rs709052 |
openSNP | rs709052 |
23andMe | rs709052 |
SNPshot | rs709052 |
SNPdbe | rs709052 |
MSV3d | rs709052 |
GWAS Ctlg | rs709052 |
GMAF | 0.4224 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs709052(C;C) rs709052(G;G) |
Alt | rs709052(C;C) rs709052(G;G) |
Reference | Rs709052(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31323233A>C; NC_000006.11:g.31323233A>G |
CLNSRC | |
CLNACC |