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rs13246321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs13246321(C;C)
Make rs13246321(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position129061277
is asnp
is mentioned by
dbSNPrs13246321
ebirs13246321
HLIrs13246321
Exacrs13246321
Varsomers13246321
Maprs13246321
PheGenIrs13246321
hapmaprs13246321
1000 genomesrs13246321
hgdprs13246321
ensemblrs13246321
gopubmedrs13246321
geneviewrs13246321
scholarrs13246321
googlers13246321
pharmgkbrs13246321
gwascentralrs13246321
openSNPrs13246321
23andMers13246321
23andMe allrs13246321
SNP Nexus

SNPshotrs13246321
SNPdbers13246321
MSV3drs13246321
GWAS Ctlgrs13246321
GMAF0.05464
Max Magnitude0
? (C;C) (C;T) (T;T) 28
According to 23andMe, this SNP is associated with Sjögren's syndrome. [PMID 20861858]