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rs397516913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516913(-;-)
Make rs397516913(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position7567786
GeneDSP
is asnp
is mentioned by
dbSNPrs397516913
ebirs397516913
HLIrs397516913
Exacrs397516913
Varsomers397516913
Maprs397516913
PheGenIrs397516913
hapmaprs397516913
1000 genomesrs397516913
hgdprs397516913
ensemblrs397516913
gopubmedrs397516913
geneviewrs397516913
scholarrs397516913
googlers397516913
pharmgkbrs397516913
gwascentralrs397516913
openSNPrs397516913
23andMers397516913
23andMe allrs397516913
SNP Nexus

SNPshotrs397516913
SNPdbers397516913
MSV3drs397516913
GWAS Ctlgrs397516913
Max Magnitude0
ClinVar
Risk rs397516913(;)
Alt rs397516913(;)
Reference rs397516913(T;T)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000006.11:g.7568019delT
CLNSRC ClinVar
CLNACC RCV000037985.3, RCV000181360.1,