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rs17796783

From SNPedia

Orientationplus
Stabilizedplus
Make rs17796783(C;C)
Make rs17796783(C;T)
Make rs17796783(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position85343567
is asnp
is mentioned by
dbSNPrs17796783
ebirs17796783
HLIrs17796783
Exacrs17796783
Varsomers17796783
Maprs17796783
PheGenIrs17796783
hapmaprs17796783
1000 genomesrs17796783
hgdprs17796783
ensemblrs17796783
gopubmedrs17796783
geneviewrs17796783
scholarrs17796783
googlers17796783
pharmgkbrs17796783
gwascentralrs17796783
openSNPrs17796783
23andMers17796783
23andMe allrs17796783
SNP Nexus

SNPshotrs17796783
SNPdbers17796783
MSV3drs17796783
GWAS Ctlgrs17796783
GMAF0.2066
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23583979OA-icon.png]
Trait Heart rate
Title Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Risk Allele T
P-val 3E-13
Odds Ratio .33 [0.24-0.43] unit increase
? (C;C) (C;T) (T;T)