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rs786205360

From SNPedia

Orientationminus
Geno Mag Summary
(GGA;GGA) 0 common in clinvar
Make rs786205360(-;-)
Make rs786205360(-;AGG)
Make rs786205360(AGG;AGG)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position31069036
GeneDSC2
is asnp
is mentioned by
dbSNPrs786205360
ebirs786205360
HLIrs786205360
Exacrs786205360
Varsomers786205360
Maprs786205360
PheGenIrs786205360
hapmaprs786205360
1000 genomesrs786205360
hgdprs786205360
ensemblrs786205360
gopubmedrs786205360
geneviewrs786205360
scholarrs786205360
googlers786205360
pharmgkbrs786205360
gwascentralrs786205360
openSNPrs786205360
23andMers786205360
23andMe allrs786205360
SNP Nexus

SNPshotrs786205360
SNPdbers786205360
MSV3drs786205360
GWAS Ctlgrs786205360
Max Magnitude0
ClinVar
Risk rs786205360(;)
Alt rs786205360(;)
Reference rs786205360(GGA;GGA)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSC2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000018.9:g.28649002_28649004delCCT
CLNSRC
CLNACC RCV000171831.2,