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rs757092

From SNPedia

Orientationplus
Stabilizedplus
Make rs757092(A;A)
Make rs757092(A;G)
Make rs757092(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2477948
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs757092
ebirs757092
HLIrs757092
Exacrs757092
Varsomers757092
Maprs757092
PheGenIrs757092
hapmaprs757092
1000 genomesrs757092
hgdprs757092
ensemblrs757092
gopubmedrs757092
geneviewrs757092
scholarrs757092
googlers757092
pharmgkbrs757092
gwascentralrs757092
openSNPrs757092
23andMers757092
23andMe allrs757092
SNP Nexus

SNPshotrs757092
SNPdbers757092
MSV3drs757092
GWAS Ctlgrs757092
GMAF0.4789
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19305408OA-icon.png] Common variants at ten loci influence QT interval duration in the QTGEN Study.


GET Evidence
rs757092
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.53125
summary