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rs11756438

From SNPedia

Orientationplus
Stabilizedplus
Make rs11756438(A;A)
Make rs11756438(A;C)
Make rs11756438(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position118672469
GeneCEP85L
is asnp
is mentioned by
dbSNPrs11756438
ebirs11756438
HLIrs11756438
Exacrs11756438
Varsomers11756438
Maprs11756438
PheGenIrs11756438
hapmaprs11756438
1000 genomesrs11756438
hgdprs11756438
ensemblrs11756438
gopubmedrs11756438
geneviewrs11756438
scholarrs11756438
googlers11756438
pharmgkbrs11756438
gwascentralrs11756438
openSNPrs11756438
23andMers11756438
23andMe allrs11756438
SNP Nexus

SNPshotrs11756438
SNPdbers11756438
MSV3drs11756438
GWAS Ctlgrs11756438
GMAF0.3646
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 5E-22
Odds Ratio 1.40 [1.06-1.74] msec increase



GET Evidence
rs11756438
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.404762
summary