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rs786204293

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204293(-;-)
Make rs786204293(-;A)
Make rs786204293(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7568462
GeneDSP
is asnp
is mentioned by
dbSNPrs786204293
ebirs786204293
HLIrs786204293
Exacrs786204293
Varsomers786204293
Maprs786204293
PheGenIrs786204293
hapmaprs786204293
1000 genomesrs786204293
hgdprs786204293
ensemblrs786204293
gopubmedrs786204293
geneviewrs786204293
scholarrs786204293
googlers786204293
pharmgkbrs786204293
gwascentralrs786204293
openSNPrs786204293
23andMers786204293
23andMe allrs786204293
SNP Nexus

SNPshotrs786204293
SNPdbers786204293
MSV3drs786204293
GWAS Ctlgrs786204293
Max Magnitude0
ClinVar
Risk rs786204293(A;A)
Alt rs786204293(A;A)
Reference rs786204293(;)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8 not provided
Reversed 0
HGVS NC_000006.11:g.7568695dupA
CLNSRC
CLNACC RCV000168639.1, RCV000181361.1,