Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516946(C;T)
Make rs397516946(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7582690
GeneDSP
is asnp
is mentioned by
dbSNPrs397516946
ebirs397516946
HLIrs397516946
Exacrs397516946
Varsomers397516946
Maprs397516946
PheGenIrs397516946
hapmaprs397516946
1000 genomesrs397516946
hgdprs397516946
ensemblrs397516946
gopubmedrs397516946
geneviewrs397516946
scholarrs397516946
googlers397516946
pharmgkbrs397516946
gwascentralrs397516946
openSNPrs397516946
23andMers397516946
23andMe allrs397516946
SNP Nexus

SNPshotrs397516946
SNPdbers397516946
MSV3drs397516946
GWAS Ctlgrs397516946
Max Magnitude0
ClinVar
Risk rs397516946(T;T)
Alt rs397516946(T;T)
Reference rs397516946(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.7582923C>T
CLNSRC ClinVar
CLNACC RCV000038064.2,