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rs148894066

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148894066(C;T)
Make rs148894066(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7579697
GeneDSP
is asnp
is mentioned by
dbSNPrs148894066
ebirs148894066
HLIrs148894066
Exacrs148894066
Varsomers148894066
Maprs148894066
PheGenIrs148894066
hapmaprs148894066
1000 genomesrs148894066
hgdprs148894066
ensemblrs148894066
gopubmedrs148894066
geneviewrs148894066
scholarrs148894066
googlers148894066
pharmgkbrs148894066
gwascentralrs148894066
openSNPrs148894066
23andMers148894066
23andMe allrs148894066
SNP Nexus

SNPshotrs148894066
SNPdbers148894066
MSV3drs148894066
GWAS Ctlgrs148894066
Max Magnitude0
ClinVar
Risk rs148894066(T;T)
Alt rs148894066(T;T)
Reference rs148894066(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000006.11:g.7579930C>A; NC_000006.11:g.7579930C>T
CLNSRC
CLNACC RCV000218217.1, RCV000155792.1,