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rs2074518

From SNPedia

Orientationminus
Stabilizedminus
Make rs2074518(A;A)
Make rs2074518(A;G)
Make rs2074518(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position34997363
GeneLIG3
is asnp
is mentioned by
dbSNPrs2074518
ebirs2074518
HLIrs2074518
Exacrs2074518
Varsomers2074518
Maprs2074518
PheGenIrs2074518
hapmaprs2074518
1000 genomesrs2074518
hgdprs2074518
ensemblrs2074518
gopubmedrs2074518
geneviewrs2074518
scholarrs2074518
googlers2074518
pharmgkbrs2074518
gwascentralrs2074518
openSNPrs2074518
23andMers2074518
23andMe allrs2074518
SNP Nexus

SNPshotrs2074518
SNPdbers2074518
MSV3drs2074518
GWAS Ctlgrs2074518
GMAF0.3255
Max Magnitude
? (A;A) (A;G) (G;G) 28

23andMe blog Influences QT interval

GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele T
P-val 6E-12
Odds Ratio



GET Evidence
rs2074518
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary