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rs17020136

From SNPedia

Orientationplus
Stabilizedplus
Make rs17020136(C;C)
Make rs17020136(C;T)
Make rs17020136(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position37020872
GeneHEATR5B
is asnp
is mentioned by
dbSNPrs17020136
ebirs17020136
HLIrs17020136
Exacrs17020136
Varsomers17020136
Maprs17020136
PheGenIrs17020136
hapmaprs17020136
1000 genomesrs17020136
hgdprs17020136
ensemblrs17020136
gopubmedrs17020136
geneviewrs17020136
scholarrs17020136
googlers17020136
pharmgkbrs17020136
gwascentralrs17020136
openSNPrs17020136
23andMers17020136
23andMe allrs17020136
SNP Nexus

SNPshotrs17020136
SNPdbers17020136
MSV3drs17020136
GWAS Ctlgrs17020136
GMAF0.2635
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele C
P-val 2E-9
Odds Ratio 0.5100 [0.35-0.67] ms increase

[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease