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rs11970286

From SNPedia

Orientationplus
Stabilizedplus
Make rs11970286(C;C)
Make rs11970286(C;T)
Make rs11970286(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position118359211
is asnp
is mentioned by
dbSNPrs11970286
ebirs11970286
HLIrs11970286
Exacrs11970286
Varsomers11970286
Maprs11970286
PheGenIrs11970286
hapmaprs11970286
1000 genomesrs11970286
hgdprs11970286
ensemblrs11970286
gopubmedrs11970286
geneviewrs11970286
scholarrs11970286
googlers11970286
pharmgkbrs11970286
gwascentralrs11970286
openSNPrs11970286
23andMers11970286
23andMe allrs11970286
SNP Nexus

SNPshotrs11970286
SNPdbers11970286
MSV3drs11970286
GWAS Ctlgrs11970286
GMAF0.3095
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele T
P-val 2E-24
Odds Ratio 1.64 [1.25-2.03] ms increase


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 8E-7
Odds Ratio 6.19 [3.73-8.65] % SD increase


GET Evidence
rs11970286
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary