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rs876657635

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657635(G;T)
Make rs876657635(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position115702996
GeneCASQ2
is asnp
is mentioned by
dbSNPrs876657635
ebirs876657635
HLIrs876657635
Exacrs876657635
Varsomers876657635
Maprs876657635
PheGenIrs876657635
hapmaprs876657635
1000 genomesrs876657635
hgdprs876657635
ensemblrs876657635
gopubmedrs876657635
geneviewrs876657635
scholarrs876657635
googlers876657635
pharmgkbrs876657635
gwascentralrs876657635
openSNPrs876657635
23andMers876657635
23andMe allrs876657635
SNP Nexus

SNPshotrs876657635
SNPdbers876657635
MSV3drs876657635
GWAS Ctlgrs876657635
Max Magnitude0
ClinVar
Risk rs876657635(T;T)
Alt rs876657635(T;T)
Reference rs876657635(G;G)
Significance Probable-Pathogenic
Disease Catecholaminergic polymorphic ventricular tachycardia
Variation info
Gene CASQ2
CLNDBN Catecholaminergic polymorphic ventricular tachycardia
Reversed 1
HGVS NC_000001.10:g.116245617C>A
CLNSRC
CLNACC RCV000222785.1,