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rs4657178

From SNPedia

Orientationplus
Stabilizedplus
Make rs4657178(C;C)
Make rs4657178(C;T)
Make rs4657178(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position162240820
GeneNOS1AP
is asnp
is mentioned by
dbSNPrs4657178
ebirs4657178
HLIrs4657178
Exacrs4657178
Varsomers4657178
Maprs4657178
PheGenIrs4657178
hapmaprs4657178
1000 genomesrs4657178
hgdprs4657178
ensemblrs4657178
gopubmedrs4657178
geneviewrs4657178
scholarrs4657178
googlers4657178
pharmgkbrs4657178
gwascentralrs4657178
openSNPrs4657178
23andMers4657178
23andMe allrs4657178
SNP Nexus

SNPshotrs4657178
SNPdbers4657178
MSV3drs4657178
GWAS Ctlgrs4657178
GMAF0.3797
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 7E-33
Odds Ratio 2.19 [1.76-2.62] ms increase



GET Evidence
rs4657178
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary