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rs397516933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516933(C;T)
Make rs397516933(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7580019
GeneDSP
is asnp
is mentioned by
dbSNPrs397516933
ebirs397516933
HLIrs397516933
Exacrs397516933
Varsomers397516933
Maprs397516933
PheGenIrs397516933
hapmaprs397516933
1000 genomesrs397516933
hgdprs397516933
ensemblrs397516933
gopubmedrs397516933
geneviewrs397516933
scholarrs397516933
googlers397516933
pharmgkbrs397516933
gwascentralrs397516933
openSNPrs397516933
23andMers397516933
23andMe allrs397516933
SNP Nexus

SNPshotrs397516933
SNPdbers397516933
MSV3drs397516933
GWAS Ctlgrs397516933
Max Magnitude0
ClinVar
Risk rs397516933(T;T)
Alt rs397516933(T;T)
Reference rs397516933(C;C)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7580252C>T
CLNSRC ClinVar
CLNACC RCV000038031.2,