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rs397516706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397516706(-;-)
Make rs397516706(-;AG)
ReferenceGRCh38 38.1/141
Chromosome18
Position31546447
GeneDSG2, RP11-75N4.2
is asnp
is mentioned by
dbSNPrs397516706
ebirs397516706
HLIrs397516706
Exacrs397516706
Varsomers397516706
Maprs397516706
PheGenIrs397516706
hapmaprs397516706
1000 genomesrs397516706
hgdprs397516706
ensemblrs397516706
gopubmedrs397516706
geneviewrs397516706
scholarrs397516706
googlers397516706
pharmgkbrs397516706
gwascentralrs397516706
openSNPrs397516706
23andMers397516706
23andMe allrs397516706
SNP Nexus

SNPshotrs397516706
SNPdbers397516706
MSV3drs397516706
GWAS Ctlgrs397516706
Max Magnitude0
ClinVar
Risk rs397516706(;)
Alt rs397516706(;)
Reference rs397516706(AG;AG)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2-AS1 DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29126410_29126411delAG
CLNSRC ClinVar
CLNACC RCV000037297.2,