rs28367580
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs28367580(C;G) |
Make rs28367580(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271380 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs28367580 |
dbSNP (classic) | rs28367580 |
ClinGen | rs28367580 |
ebi | rs28367580 |
HLI | rs28367580 |
Exac | rs28367580 |
Gnomad | rs28367580 |
Varsome | rs28367580 |
LitVar | rs28367580 |
Map | rs28367580 |
PheGenI | rs28367580 |
Biobank | rs28367580 |
1000 genomes | rs28367580 |
hgdp | rs28367580 |
ensembl | rs28367580 |
geneview | rs28367580 |
scholar | rs28367580 |
rs28367580 | |
pharmgkb | rs28367580 |
gwascentral | rs28367580 |
openSNP | rs28367580 |
23andMe | rs28367580 |
SNPshot | rs28367580 |
SNPdbe | rs28367580 |
MSV3d | rs28367580 |
GWAS Ctlg | rs28367580 |
GMAF | 0.04316 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs28367580(G;G) |
Alt | rs28367580(G;G) |
Reference | Rs28367580(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31239157C>G |
CLNSRC | |
CLNACC |