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rs730880082

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880082(C;T)
Make rs730880082(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7576986
GeneDSP
is asnp
is mentioned by
dbSNPrs730880082
ebirs730880082
HLIrs730880082
Exacrs730880082
Varsomers730880082
Maprs730880082
PheGenIrs730880082
hapmaprs730880082
1000 genomesrs730880082
hgdprs730880082
ensemblrs730880082
gopubmedrs730880082
geneviewrs730880082
scholarrs730880082
googlers730880082
pharmgkbrs730880082
gwascentralrs730880082
openSNPrs730880082
23andMers730880082
23andMe allrs730880082
SNP Nexus

SNPshotrs730880082
SNPdbers730880082
MSV3drs730880082
GWAS Ctlgrs730880082
Max Magnitude0
ClinVar
Risk rs730880082(T;T)
Alt rs730880082(T;T)
Reference rs730880082(C;C)
Significance Pathogenic
Disease Cardiac arrest Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Cardiac arrest Arrhythmogenic right ventricular cardiomyopathy, type 8 not provided
Reversed 0
HGVS NC_000006.11:g.7577219C>T
CLNSRC
CLNACC RCV000157193.1, RCV000168644.1, RCV000181308.1,