rs1055311
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1055311(C;T) |
Make rs1055311(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 44289685 |
Gene | AIRE |
is a | snp |
is | mentioned by |
dbSNP | rs1055311 |
dbSNP (classic) | rs1055311 |
ClinGen | rs1055311 |
ebi | rs1055311 |
HLI | rs1055311 |
Exac | rs1055311 |
Gnomad | rs1055311 |
Varsome | rs1055311 |
LitVar | rs1055311 |
Map | rs1055311 |
PheGenI | rs1055311 |
Biobank | rs1055311 |
1000 genomes | rs1055311 |
hgdp | rs1055311 |
ensembl | rs1055311 |
geneview | rs1055311 |
scholar | rs1055311 |
rs1055311 | |
pharmgkb | rs1055311 |
gwascentral | rs1055311 |
openSNP | rs1055311 |
23andMe | rs1055311 |
SNPshot | rs1055311 |
SNPdbe | rs1055311 |
MSV3d | rs1055311 |
GWAS Ctlg | rs1055311 |
GMAF | 0.1368 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20363194] The role of AIRE polymorphisms in melanoma
ClinVar | |
---|---|
Risk | rs1055311(G;G) rs1055311(T;T) |
Alt | rs1055311(G;G) rs1055311(T;T) |
Reference | Rs1055311(C;C) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | AIRE |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000021.8:g.45709568C>T |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000116302.3, |