rs6474
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs6474(A;A) |
Make rs6474(A;G) |
Chromosome | 6 |
Position | 32039109 |
Gene | CYP21A2 |
is a | snp |
is | mentioned by |
dbSNP | rs6474 |
dbSNP (classic) | rs6474 |
ClinGen | rs6474 |
ebi | rs6474 |
HLI | rs6474 |
Exac | rs6474 |
Gnomad | rs6474 |
Varsome | rs6474 |
LitVar | rs6474 |
Map | rs6474 |
PheGenI | rs6474 |
Biobank | rs6474 |
1000 genomes | rs6474 |
hgdp | rs6474 |
ensembl | rs6474 |
geneview | rs6474 |
scholar | rs6474 |
rs6474 | |
pharmgkb | rs6474 |
gwascentral | rs6474 |
openSNP | rs6474 |
23andMe | rs6474 |
SNPshot | rs6474 |
SNPdbe | rs6474 |
MSV3d | rs6474 |
GWAS Ctlg | rs6474 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25249698] CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
ClinVar | |
---|---|
Risk | rs6474(A;A) |
Alt | rs6474(A;A) |
Reference | Rs6474(G;G) |
Significance | Non-pathogenic |
Disease | 21-hydroxylase deficiency not specified |
Variation | info |
Gene | CYP21A2 |
CLNDBN | 21-hydroxylase deficiency not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.32006886G>A |
CLNSRC | |
CLNACC | RCV000055817.1, RCV000245772.1, |