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rs879255521

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255521(C;T)
Make rs879255521(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7580193
GeneDSP
is asnp
is mentioned by
dbSNPrs879255521
ebirs879255521
HLIrs879255521
Exacrs879255521
Varsomers879255521
Maprs879255521
PheGenIrs879255521
hapmaprs879255521
1000 genomesrs879255521
hgdprs879255521
ensemblrs879255521
gopubmedrs879255521
geneviewrs879255521
scholarrs879255521
googlers879255521
pharmgkbrs879255521
gwascentralrs879255521
openSNPrs879255521
23andMers879255521
23andMe allrs879255521
SNP Nexus

SNPshotrs879255521
SNPdbers879255521
MSV3drs879255521
GWAS Ctlgrs879255521
Max Magnitude0
ClinVar
Risk rs879255521(T;T)
Alt rs879255521(T;T)
Reference rs879255521(C;C)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy
Variation info
Gene DSP
CLNDBN Dilated cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7580426C>T
CLNSRC University Hospital of Geneva
CLNACC RCV000234860.1,