rs9264664
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs9264664(C;T) |
Make rs9264664(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271450 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs9264664 |
dbSNP (classic) | rs9264664 |
ClinGen | rs9264664 |
ebi | rs9264664 |
HLI | rs9264664 |
Exac | rs9264664 |
Gnomad | rs9264664 |
Varsome | rs9264664 |
LitVar | rs9264664 |
Map | rs9264664 |
PheGenI | rs9264664 |
Biobank | rs9264664 |
1000 genomes | rs9264664 |
hgdp | rs9264664 |
ensembl | rs9264664 |
geneview | rs9264664 |
scholar | rs9264664 |
rs9264664 | |
pharmgkb | rs9264664 |
gwascentral | rs9264664 |
openSNP | rs9264664 |
23andMe | rs9264664 |
SNPshot | rs9264664 |
SNPdbe | rs9264664 |
MSV3d | rs9264664 |
GWAS Ctlg | rs9264664 |
GMAF | 0.2585 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs9264664(T;T) |
Alt | rs9264664(T;T) |
Reference | Rs9264664(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31239227C>T |
CLNSRC | |
CLNACC |