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rs1321311

From SNPedia

Orientationminus
Stabilizedminus
Make rs1321311(G;G)
Make rs1321311(G;T)
Make rs1321311(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position36655123
is asnp
is mentioned by
dbSNPrs1321311
ebirs1321311
HLIrs1321311
Exacrs1321311
Varsomers1321311
Maprs1321311
PheGenIrs1321311
hapmaprs1321311
1000 genomesrs1321311
hgdprs1321311
ensemblrs1321311
gopubmedrs1321311
geneviewrs1321311
scholarrs1321311
googlers1321311
pharmgkbrs1321311
gwascentralrs1321311
openSNPrs1321311
23andMers1321311
23andMe allrs1321311
SNP Nexus

SNPshotrs1321311
SNPdbers1321311
MSV3drs1321311
GWAS Ctlgrs1321311
GMAF0.2475
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele T
P-val 3E-10
Odds Ratio 6.52 [4.50-8.55] % SD increase


[PMID 22634755] Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.


[PMID 26078566OA-icon.png] Association of colorectal cancer susceptibility variants with esophageal cancer in a Chinese population