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rs397517906

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517906(C;T)
Make rs397517906(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134890
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517906
ebirs397517906
HLIrs397517906
Exacrs397517906
Varsomers397517906
Maprs397517906
PheGenIrs397517906
hapmaprs397517906
1000 genomesrs397517906
hgdprs397517906
ensemblrs397517906
gopubmedrs397517906
geneviewrs397517906
scholarrs397517906
googlers397517906
pharmgkbrs397517906
gwascentralrs397517906
openSNPrs397517906
23andMers397517906
23andMe allrs397517906
SNP Nexus

SNPshotrs397517906
SNPdbers397517906
MSV3drs397517906
GWAS Ctlgrs397517906
Max Magnitude0
ClinVar
Risk rs397517906(T;T)
Alt rs397517906(T;T)
Reference rs397517906(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156104681C>T
CLNSRC
CLNACC RCV000041361.4, RCV000157293.1, RCV000182361.1,