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rs6474

From SNPedia

Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6474(A;A)
Make rs6474(A;G)
is asnp
is mentioned by
dbSNPrs6474
ebirs6474
HLIrs6474
Exacrs6474
Varsomers6474
Maprs6474
PheGenIrs6474
hapmaprs6474
1000 genomesrs6474
hgdprs6474
ensemblrs6474
gopubmedrs6474
geneviewrs6474
scholarrs6474
googlers6474
pharmgkbrs6474
gwascentralrs6474
openSNPrs6474
23andMers6474
23andMe allrs6474
SNP Nexus

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
Variation info
Gene CYP21A2
CLNDBN 21-hydroxylase deficiency
Reversed 0
HGVS NC_000006.11:g.32006886G>A
CLNSRC
CLNACC RCV000055817.1,