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rs151344502

From SNPedia

Merged intors111647200
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151344502(A;A)
Make rs151344502(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32039807
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs151344502
ebirs151344502
HLIrs151344502
Exacrs151344502
Varsomers151344502
Maprs151344502
PheGenIrs151344502
hapmaprs151344502
1000 genomesrs151344502
hgdprs151344502
ensemblrs151344502
gopubmedrs151344502
geneviewrs151344502
scholarrs151344502
googlers151344502
pharmgkbrs151344502
gwascentralrs151344502
openSNPrs151344502
23andMers151344502
23andMe allrs151344502
SNP Nexus

SNPshotrs151344502
SNPdbers151344502
MSV3drs151344502
GWAS Ctlgrs151344502
StatusMerged into rs111647200
Max Magnitude0
ClinVar
Risk rs151344502(A;A)
Alt rs151344502(A;A)
Reference rs151344502(T;T)
Significance Probable-Pathogenic
Disease
Variation info
Gene CYP21A2
CLNDBN
Reversed 0
HGVS NC_000006.11:g.32007584T>A
CLNSRC
CLNACC