rs1133779
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1133779(C;C) |
Make rs1133779(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 44297667 |
Gene | AIRE |
is a | snp |
is | mentioned by |
dbSNP | rs1133779 |
dbSNP (classic) | rs1133779 |
ClinGen | rs1133779 |
ebi | rs1133779 |
HLI | rs1133779 |
Exac | rs1133779 |
Gnomad | rs1133779 |
Varsome | rs1133779 |
LitVar | rs1133779 |
Map | rs1133779 |
PheGenI | rs1133779 |
Biobank | rs1133779 |
1000 genomes | rs1133779 |
hgdp | rs1133779 |
ensembl | rs1133779 |
geneview | rs1133779 |
scholar | rs1133779 |
rs1133779 | |
pharmgkb | rs1133779 |
gwascentral | rs1133779 |
openSNP | rs1133779 |
23andMe | rs1133779 |
SNPshot | rs1133779 |
SNPdbe | rs1133779 |
MSV3d | rs1133779 |
GWAS Ctlg | rs1133779 |
Merged from | Rs1800522 |
GMAF | 0.4573 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20363194] The role of AIRE polymorphisms in melanoma.
ClinVar | |
---|---|
Risk | rs1133779(C;C) |
Alt | rs1133779(C;C) |
Reference | Rs1133779(T;T) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | AIRE |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000021.8:g.45717550T>C |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000116300.3, |