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rs397516940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516940(C;T)
Make rs397516940(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7580721
GeneDSP
is asnp
is mentioned by
dbSNPrs397516940
ebirs397516940
HLIrs397516940
Exacrs397516940
Varsomers397516940
Maprs397516940
PheGenIrs397516940
hapmaprs397516940
1000 genomesrs397516940
hgdprs397516940
ensemblrs397516940
gopubmedrs397516940
geneviewrs397516940
scholarrs397516940
googlers397516940
pharmgkbrs397516940
gwascentralrs397516940
openSNPrs397516940
23andMers397516940
23andMe allrs397516940
SNP Nexus

SNPshotrs397516940
SNPdbers397516940
MSV3drs397516940
GWAS Ctlgrs397516940
Max Magnitude0
ClinVar
Risk rs397516940(T;T)
Alt rs397516940(T;T)
Reference rs397516940(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.7580954C>T
CLNSRC ClinVar
CLNACC RCV000038049.3,