rs6473
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs6473(A;A) |
Make rs6473(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32041127 |
Gene | CYP21A2, TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs6473 |
dbSNP (classic) | rs6473 |
ClinGen | rs6473 |
ebi | rs6473 |
HLI | rs6473 |
Exac | rs6473 |
Gnomad | rs6473 |
Varsome | rs6473 |
LitVar | rs6473 |
Map | rs6473 |
PheGenI | rs6473 |
Biobank | rs6473 |
1000 genomes | rs6473 |
hgdp | rs6473 |
ensembl | rs6473 |
geneview | rs6473 |
scholar | rs6473 |
rs6473 | |
pharmgkb | rs6473 |
gwascentral | rs6473 |
openSNP | rs6473 |
23andMe | rs6473 |
SNPshot | rs6473 |
SNPdbe | rs6473 |
MSV3d | rs6473 |
GWAS Ctlg | rs6473 |
Max Magnitude | 0 |
[PMID 25249698] CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
ClinVar | |
---|---|
Risk | rs6473(A;A) rs6473(C;C) |
Alt | rs6473(A;A) rs6473(C;C) |
Reference | Rs6473(G;G) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | TNXB CYP21A2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.32008904G>A |
CLNSRC | |
CLNACC | RCV000243232.2, |