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rs9984896

From SNPedia

Orientationplus
Stabilizedplus
Make rs9984896(A;A)
Make rs9984896(A;C)
Make rs9984896(C;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position36563371
GeneCLDN14
is asnp
is mentioned by
dbSNPrs9984896
ebirs9984896
HLIrs9984896
Exacrs9984896
Varsomers9984896
Maprs9984896
PheGenIrs9984896
hapmaprs9984896
1000 genomesrs9984896
hgdprs9984896
ensemblrs9984896
gopubmedrs9984896
geneviewrs9984896
scholarrs9984896
googlers9984896
pharmgkbrs9984896
gwascentralrs9984896
openSNPrs9984896
23andMers9984896
23andMe allrs9984896
SNP Nexus

SNPshotrs9984896
SNPdbers9984896
MSV3drs9984896
GWAS Ctlgrs9984896
GMAF0.1175
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23166209OA-icon.png]
Trait QT interval
Title Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele A
P-val 5E-6
Odds Ratio 2.85 [1.63-4.07] unit decrease