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rs1896312

From SNPedia

Orientationminus
Stabilizedminus
Make rs1896312(A;A)
Make rs1896312(A;G)
Make rs1896312(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position114908619
is asnp
is mentioned by
dbSNPrs1896312
ebirs1896312
HLIrs1896312
Exacrs1896312
Varsomers1896312
Maprs1896312
PheGenIrs1896312
hapmaprs1896312
1000 genomesrs1896312
hgdprs1896312
ensemblrs1896312
gopubmedrs1896312
geneviewrs1896312
scholarrs1896312
googlers1896312
pharmgkbrs1896312
gwascentralrs1896312
openSNPrs1896312
23andMers1896312
23andMe allrs1896312
SNP Nexus

SNPshotrs1896312
SNPdbers1896312
MSV3drs1896312
GWAS Ctlgrs1896312
GMAF0.3664
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval
Risk Allele C
P-val 3E-17
Odds Ratio 1.95 [1.50-2.40] ms increase


[PMID 21347284OA-icon.png] Genome-wide association studies of the PR interval in African Americans.