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rs397516915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516915(C;T)
Make rs397516915(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7568443
GeneDSP
is asnp
is mentioned by
dbSNPrs397516915
ebirs397516915
HLIrs397516915
Exacrs397516915
Varsomers397516915
Maprs397516915
PheGenIrs397516915
hapmaprs397516915
1000 genomesrs397516915
hgdprs397516915
ensemblrs397516915
gopubmedrs397516915
geneviewrs397516915
scholarrs397516915
googlers397516915
pharmgkbrs397516915
gwascentralrs397516915
openSNPrs397516915
23andMers397516915
23andMe allrs397516915
SNP Nexus

SNPshotrs397516915
SNPdbers397516915
MSV3drs397516915
GWAS Ctlgrs397516915
Max Magnitude0
ClinVar
Risk rs397516915(T;T)
Alt rs397516915(T;T)
Reference rs397516915(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.7568676C>T
CLNSRC ClinVar
CLNACC RCV000208168.2,