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rs7521023

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7521023(A;A)
Make rs7521023(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position115700759
GeneCASQ2
is asnp
is mentioned by
dbSNPrs7521023
dbSNP (old)rs7521023
ClinGenrs7521023
ebirs7521023
HLIrs7521023
Exacrs7521023
Varsomers7521023
Maprs7521023
PheGenIrs7521023
Biobankrs7521023
1000 genomesrs7521023
hgdprs7521023
ensemblrs7521023
gopubmedrs7521023
geneviewrs7521023
scholarrs7521023
googlers7521023
pharmgkbrs7521023
gwascentralrs7521023
openSNPrs7521023
23andMers7521023
23andMe allrs7521023
SNP Nexus

SNPshotrs7521023
SNPdbers7521023
MSV3drs7521023
GWAS Ctlgrs7521023
GMAF0.3118
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 24444446OA-icon.png] Association of CASQ2 Polymorphisms With Sudden Cardiac Arrest and Heart Failure in Patients with Coronary Artery Disease


ClinVar
Risk rs7521023(A;A)
Alt rs7521023(A;A)
Reference Rs7521023(G;G)
Significance Probable-non-pathogenic
Disease Catecholaminergic polymorphic ventricular tachycardia Neural tube defect Caudal dysgenesis syndrome
Variation info
Gene CASQ2
CLNDBN Catecholaminergic polymorphic ventricular tachycardia Neural tube defect Caudal dysgenesis syndrome
Reversed 0
HGVS NC_000001.10:g.116243380G>A
CLNSRC
CLNACC RCV000264813.1, RCV000272946.1, RCV000330414.1,