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rs397517907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517907(C;T)
Make rs397517907(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134914
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517907
ebirs397517907
HLIrs397517907
Exacrs397517907
Varsomers397517907
Maprs397517907
PheGenIrs397517907
hapmaprs397517907
1000 genomesrs397517907
hgdprs397517907
ensemblrs397517907
gopubmedrs397517907
geneviewrs397517907
scholarrs397517907
googlers397517907
pharmgkbrs397517907
gwascentralrs397517907
openSNPrs397517907
23andMers397517907
23andMe allrs397517907
SNP Nexus

SNPshotrs397517907
SNPdbers397517907
MSV3drs397517907
GWAS Ctlgrs397517907
Max Magnitude0
ClinVar
Risk rs397517907(T;T)
Alt rs397517907(T;T)
Reference rs397517907(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000001.10:g.156104705C>T
CLNSRC ClinVar
CLNACC RCV000041363.2, RCV000237089.1,