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rs730880092

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880092(-;-)
Make rs730880092(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7583572
GeneDSP
is asnp
is mentioned by
dbSNPrs730880092
ebirs730880092
HLIrs730880092
Exacrs730880092
Varsomers730880092
Maprs730880092
PheGenIrs730880092
hapmaprs730880092
1000 genomesrs730880092
hgdprs730880092
ensemblrs730880092
gopubmedrs730880092
geneviewrs730880092
scholarrs730880092
googlers730880092
pharmgkbrs730880092
gwascentralrs730880092
openSNPrs730880092
23andMers730880092
23andMe allrs730880092
SNP Nexus

SNPshotrs730880092
SNPdbers730880092
MSV3drs730880092
GWAS Ctlgrs730880092
Max Magnitude0
ClinVar
Risk rs730880092(;)
Alt rs730880092(;)
Reference rs730880092(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSP
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7583805delA
CLNSRC
CLNACC RCV000157216.2,