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rs786204299

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204299(-;-)
Make rs786204299(-;C)
Make rs786204299(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position7583672
GeneDSP
is asnp
is mentioned by
dbSNPrs786204299
ebirs786204299
HLIrs786204299
Exacrs786204299
Varsomers786204299
Maprs786204299
PheGenIrs786204299
hapmaprs786204299
1000 genomesrs786204299
hgdprs786204299
ensemblrs786204299
gopubmedrs786204299
geneviewrs786204299
scholarrs786204299
googlers786204299
pharmgkbrs786204299
gwascentralrs786204299
openSNPrs786204299
23andMers786204299
23andMe allrs786204299
SNP Nexus

SNPshotrs786204299
SNPdbers786204299
MSV3drs786204299
GWAS Ctlgrs786204299
Max Magnitude0
ClinVar
Risk rs786204299(C;C)
Alt rs786204299(C;C)
Reference rs786204299(;)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8
Reversed 0
HGVS NC_000006.11:g.7583905dupC
CLNSRC
CLNACC RCV000168653.1,