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rs796052171

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052171(A;T)
Make rs796052171(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position8733913
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs796052171
ebirs796052171
HLIrs796052171
Exacrs796052171
Varsomers796052171
Maprs796052171
PheGenIrs796052171
hapmaprs796052171
1000 genomesrs796052171
hgdprs796052171
ensemblrs796052171
gopubmedrs796052171
geneviewrs796052171
scholarrs796052171
googlers796052171
pharmgkbrs796052171
gwascentralrs796052171
openSNPrs796052171
23andMers796052171
23andMe allrs796052171
SNP Nexus

SNPshotrs796052171
SNPdbers796052171
MSV3drs796052171
GWAS Ctlgrs796052171
Max Magnitude0
ClinVar
Risk rs796052171(T;T)
Alt rs796052171(T;T)
Reference rs796052171(A;A)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene SSUH2 CAV3
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000003.11:g.8775599A>T
CLNSRC
CLNACC RCV000190168.1,