Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880093

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880093(-;-)
Make rs730880093(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7583655
GeneDSP
is asnp
is mentioned by
dbSNPrs730880093
ebirs730880093
HLIrs730880093
Exacrs730880093
Varsomers730880093
Maprs730880093
PheGenIrs730880093
hapmaprs730880093
1000 genomesrs730880093
hgdprs730880093
ensemblrs730880093
gopubmedrs730880093
geneviewrs730880093
scholarrs730880093
googlers730880093
pharmgkbrs730880093
gwascentralrs730880093
openSNPrs730880093
23andMers730880093
23andMe allrs730880093
SNP Nexus

SNPshotrs730880093
SNPdbers730880093
MSV3drs730880093
GWAS Ctlgrs730880093
Max Magnitude0
ClinVar
Risk rs730880093(;)
Alt rs730880093(;)
Reference rs730880093(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7583888delA
CLNSRC
CLNACC RCV000157217.1,