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rs397516955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516955(A;A)
Make rs397516955(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position7562753
GeneDSP
is asnp
is mentioned by
dbSNPrs397516955
ebirs397516955
HLIrs397516955
Exacrs397516955
Varsomers397516955
Maprs397516955
PheGenIrs397516955
hapmaprs397516955
1000 genomesrs397516955
hgdprs397516955
ensemblrs397516955
gopubmedrs397516955
geneviewrs397516955
scholarrs397516955
googlers397516955
pharmgkbrs397516955
gwascentralrs397516955
openSNPrs397516955
23andMers397516955
23andMe allrs397516955
SNP Nexus

SNPshotrs397516955
SNPdbers397516955
MSV3drs397516955
GWAS Ctlgrs397516955
Max Magnitude0
ClinVar
Risk rs397516955(A;A)
Alt rs397516955(A;A)
Reference rs397516955(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSP
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7562986G>A
CLNSRC ClinVar
CLNACC RCV000038082.3,