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rs397516923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516923(C;T)
Make rs397516923(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7555761
GeneDSP
is asnp
is mentioned by
dbSNPrs397516923
ebirs397516923
HLIrs397516923
Exacrs397516923
Varsomers397516923
Maprs397516923
PheGenIrs397516923
hapmaprs397516923
1000 genomesrs397516923
hgdprs397516923
ensemblrs397516923
gopubmedrs397516923
geneviewrs397516923
scholarrs397516923
googlers397516923
pharmgkbrs397516923
gwascentralrs397516923
openSNPrs397516923
23andMers397516923
23andMe allrs397516923
SNP Nexus

SNPshotrs397516923
SNPdbers397516923
MSV3drs397516923
GWAS Ctlgrs397516923
Max Magnitude0
ClinVar
Risk rs397516923(T;T)
Alt rs397516923(T;T)
Reference rs397516923(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.7555994C>T
CLNSRC ClinVar
CLNACC RCV000038006.2,