rs11547346
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs11547346(A;C) |
Make rs11547346(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271569 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs11547346 |
dbSNP (classic) | rs11547346 |
ClinGen | rs11547346 |
ebi | rs11547346 |
HLI | rs11547346 |
Exac | rs11547346 |
Gnomad | rs11547346 |
Varsome | rs11547346 |
LitVar | rs11547346 |
Map | rs11547346 |
PheGenI | rs11547346 |
Biobank | rs11547346 |
1000 genomes | rs11547346 |
hgdp | rs11547346 |
ensembl | rs11547346 |
geneview | rs11547346 |
scholar | rs11547346 |
rs11547346 | |
pharmgkb | rs11547346 |
gwascentral | rs11547346 |
openSNP | rs11547346 |
23andMe | rs11547346 |
SNPshot | rs11547346 |
SNPdbe | rs11547346 |
MSV3d | rs11547346 |
GWAS Ctlg | rs11547346 |
GMAF | 0.03352 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11547346(C;C) |
Alt | rs11547346(C;C) |
Reference | Rs11547346(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31239346T>G |
CLNSRC | |
CLNACC |