rs61759951
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs61759951(C;C) |
Make rs61759951(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355507 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs61759951 |
dbSNP (classic) | rs61759951 |
ClinGen | rs61759951 |
ebi | rs61759951 |
HLI | rs61759951 |
Exac | rs61759951 |
Gnomad | rs61759951 |
Varsome | rs61759951 |
LitVar | rs61759951 |
Map | rs61759951 |
PheGenI | rs61759951 |
Biobank | rs61759951 |
1000 genomes | rs61759951 |
hgdp | rs61759951 |
ensembl | rs61759951 |
geneview | rs61759951 |
scholar | rs61759951 |
rs61759951 | |
pharmgkb | rs61759951 |
gwascentral | rs61759951 |
openSNP | rs61759951 |
23andMe | rs61759951 |
SNPshot | rs61759951 |
SNPdbe | rs61759951 |
MSV3d | rs61759951 |
GWAS Ctlg | rs61759951 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61759951(C;C) |
Alt | rs61759951(C;C) |
Reference | Rs61759951(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31323284C>G |
CLNSRC | |
CLNACC |