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rs397516932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAACAAAT;AAGAACAAAT) 0 common in clinvar
(AATAAGAACA;AATAAGAACA) 0 common in clinvar
Make rs397516932(-;-)
Make rs397516932(-;AAGAACAAAT)
ReferenceGRCh38 38.1/141
Chromosome6
Position7579350
GeneDSP
is asnp
is mentioned by
dbSNPrs397516932
ebirs397516932
HLIrs397516932
Exacrs397516932
Varsomers397516932
Maprs397516932
PheGenIrs397516932
hapmaprs397516932
1000 genomesrs397516932
hgdprs397516932
ensemblrs397516932
gopubmedrs397516932
geneviewrs397516932
scholarrs397516932
googlers397516932
pharmgkbrs397516932
gwascentralrs397516932
openSNPrs397516932
23andMers397516932
23andMe allrs397516932
SNP Nexus

SNPshotrs397516932
SNPdbers397516932
MSV3drs397516932
GWAS Ctlgrs397516932
Max Magnitude0
ClinVar
Risk rs397516932(;)
Alt rs397516932(;)
Reference rs397516932(AATAAGAACA;AATAAGAACA)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7579583_7579592delAAGAACAAAT
CLNSRC ClinVar
CLNACC RCV000038027.2,