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rs6473

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6473(A;A)
Make rs6473(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32041127
GeneCYP21A2, TNXB
is asnp
is mentioned by
dbSNPrs6473
ebirs6473
HLIrs6473
Exacrs6473
Varsomers6473
Maprs6473
PheGenIrs6473
hapmaprs6473
1000 genomesrs6473
hgdprs6473
ensemblrs6473
gopubmedrs6473
geneviewrs6473
scholarrs6473
googlers6473
pharmgkbrs6473
gwascentralrs6473
openSNPrs6473
23andMers6473
23andMe allrs6473
SNP Nexus

SNPshotrs6473
SNPdbers6473
MSV3drs6473
GWAS Ctlgrs6473
Max Magnitude0

[PMID 25249698] CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles

ClinVar
Risk rs6473(A,C;A,C)
Alt rs6473(A,C;A,C)
Reference rs6473(G;G)
Significance Unknown
Disease not provided
Variation info
Gene TNXB CYP21A2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.32008904G>A
CLNSRC
CLNACC RCV000173701.1,