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rs8049607

From SNPedia

Orientationplus
Stabilizedplus
Make rs8049607(C;C)
Make rs8049607(C;T)
Make rs8049607(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11597897
is asnp
is mentioned by
dbSNPrs8049607
ebirs8049607
HLIrs8049607
Exacrs8049607
Varsomers8049607
Maprs8049607
PheGenIrs8049607
hapmaprs8049607
1000 genomesrs8049607
hgdprs8049607
ensemblrs8049607
gopubmedrs8049607
geneviewrs8049607
scholarrs8049607
googlers8049607
pharmgkbrs8049607
gwascentralrs8049607
openSNPrs8049607
23andMers8049607
23andMe allrs8049607
SNP Nexus

SNPshotrs8049607
SNPdbers8049607
MSV3drs8049607
GWAS Ctlgrs8049607
GMAF0.4977
Max Magnitude
? (C;C) (C;T) (T;T) 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 5E-15
Odds Ratio
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 6E-15
Odds Ratio 1.25 [0.81-1.69] ms increase




GET Evidence
rs8049607
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.53125
summary



GWAS snp
PMID [PMID 23166209OA-icon.png]
Trait QT interval
Title Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele C
P-val 7E-7
Odds Ratio 1.63 [0.98-2.28] unit decrease