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rs6474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6474(A;A)
Make rs6474(A;G)
Chromosome6
Position32039109
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs6474
dbSNP (classic)rs6474
ClinGenrs6474
ebirs6474
HLIrs6474
Exacrs6474
Gnomadrs6474
Varsomers6474
LitVarrs6474
Maprs6474
PheGenIrs6474
Biobankrs6474
1000 genomesrs6474
hgdprs6474
ensemblrs6474
geneviewrs6474
scholarrs6474
googlers6474
pharmgkbrs6474
gwascentralrs6474
openSNPrs6474
23andMers6474
SNPshotrs6474
SNPdbers6474
MSV3drs6474
GWAS Ctlgrs6474
Max Magnitude0
? (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,