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rs763955301

From SNPedia

Orientationplus
Make rs763955301(-;-)
Make rs763955301(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position115732961
GeneCASQ2
is asnp
is mentioned by
dbSNPrs763955301
ebirs763955301
HLIrs763955301
Exacrs763955301
Varsomers763955301
Maprs763955301
PheGenIrs763955301
hapmaprs763955301
1000 genomesrs763955301
hgdprs763955301
ensemblrs763955301
gopubmedrs763955301
geneviewrs763955301
scholarrs763955301
googlers763955301
pharmgkbrs763955301
gwascentralrs763955301
openSNPrs763955301
23andMers763955301
23andMe allrs763955301
SNP Nexus

SNPshotrs763955301
SNPdbers763955301
MSV3drs763955301
GWAS Ctlgrs763955301
Max Magnitude
ClinVar
Risk rs763955301(;)
Alt rs763955301(;)
Reference rs763955301(A;A)
Significance Probable-Pathogenic
Disease Ventricular tachycardia
Variation info
Gene CASQ2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.116275582delA
CLNSRC
CLNACC RCV000208054.1,