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rs219778

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs219778(C;C)
Make rs219778(C;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position36462343
GeneCLDN14
is asnp
is mentioned by
dbSNPrs219778
ebirs219778
HLIrs219778
Exacrs219778
Varsomers219778
Maprs219778
PheGenIrs219778
hapmaprs219778
1000 genomesrs219778
hgdprs219778
ensemblrs219778
gopubmedrs219778
geneviewrs219778
scholarrs219778
googlers219778
pharmgkbrs219778
gwascentralrs219778
openSNPrs219778
23andMers219778
23andMe allrs219778
SNP Nexus

SNPshotrs219778
SNPdbers219778
MSV3drs219778
GWAS Ctlgrs219778
GMAF0.253
Max Magnitude0
? (C;C) (C;T) (T;T) 28
DeCode reports that carriers of two T alleles at rs219778 have a slightly increased risk of developing kidney stones. [PMID 19561606]