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rs397516943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516943(C;T)
Make rs397516943(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7559281
GeneDSP
is asnp
is mentioned by
dbSNPrs397516943
ebirs397516943
HLIrs397516943
Exacrs397516943
Varsomers397516943
Maprs397516943
PheGenIrs397516943
hapmaprs397516943
1000 genomesrs397516943
hgdprs397516943
ensemblrs397516943
gopubmedrs397516943
geneviewrs397516943
scholarrs397516943
googlers397516943
pharmgkbrs397516943
gwascentralrs397516943
openSNPrs397516943
23andMers397516943
23andMe allrs397516943
SNP Nexus

SNPshotrs397516943
SNPdbers397516943
MSV3drs397516943
GWAS Ctlgrs397516943
Max Magnitude0
ClinVar
Risk rs397516943(T;T)
Alt rs397516943(T;T)
Reference rs397516943(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 0
HGVS NC_000006.11:g.7559514C>T
CLNSRC ClinVar
CLNACC RCV000038058.3, RCV000181275.2,