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rs367752002

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs367752002(A;G)
Make rs367752002(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7576347
GeneDSP
is asnp
is mentioned by
dbSNPrs367752002
ebirs367752002
HLIrs367752002
Exacrs367752002
Varsomers367752002
Maprs367752002
PheGenIrs367752002
hapmaprs367752002
1000 genomesrs367752002
hgdprs367752002
ensemblrs367752002
gopubmedrs367752002
geneviewrs367752002
scholarrs367752002
googlers367752002
pharmgkbrs367752002
gwascentralrs367752002
openSNPrs367752002
23andMers367752002
23andMe allrs367752002
SNP Nexus

SNPshotrs367752002
SNPdbers367752002
MSV3drs367752002
GWAS Ctlgrs367752002
Max Magnitude0
ClinVar
Risk rs367752002(C,G;C,G)
Alt rs367752002(C,G;C,G)
Reference rs367752002(A;A)
Significance Probable-Pathogenic
Disease not specified Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN not specified Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 0
HGVS NC_000006.11:g.7576580A>G
CLNSRC
CLNACC RCV000150562.1, RCV000157192.1, RCV000171390.3,