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rs4074536

From SNPedia

Orientationplus
Stabilizedplus
Make rs4074536(C;C)
Make rs4074536(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115768346
GeneCASQ2
is asnp
is mentioned by
dbSNPrs4074536
ebirs4074536
HLIrs4074536
Exacrs4074536
Varsomers4074536
Maprs4074536
PheGenIrs4074536
hapmaprs4074536
1000 genomesrs4074536
hgdprs4074536
ensemblrs4074536
gopubmedrs4074536
geneviewrs4074536
scholarrs4074536
googlers4074536
pharmgkbrs4074536
gwascentralrs4074536
openSNPrs4074536
23andMers4074536
23andMe allrs4074536
SNP Nexus

SNPshotrs4074536
SNPdbers4074536
MSV3drs4074536
GWAS Ctlgrs4074536
GMAF0.4137
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele C
P-val 2E-8
Odds Ratio 0.4200 [0.28-0.56] ms decrease


GET Evidence
CASQ2-T66A
aa_change Thr66Ala
aa_change_short T66A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.34235
summary



ClinVar
Risk rs4074536(C;C)
Alt rs4074536(C;C)
Reference rs4074536(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CASQ2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.116310967T>C
CLNSRC ClinVar
CLNACC RCV000037136.3,