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rs58917027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs58917027(A;C)
Make rs58917027(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position156130708
GeneLMNA
is asnp
is mentioned by
dbSNPrs58917027
ebirs58917027
HLIrs58917027
Exacrs58917027
Varsomers58917027
Maprs58917027
PheGenIrs58917027
hapmaprs58917027
1000 genomesrs58917027
hgdprs58917027
ensemblrs58917027
gopubmedrs58917027
geneviewrs58917027
scholarrs58917027
googlers58917027
pharmgkbrs58917027
gwascentralrs58917027
openSNPrs58917027
23andMers58917027
23andMe allrs58917027
SNP Nexus

SNPshotrs58917027
SNPdbers58917027
MSV3drs58917027
GWAS Ctlgrs58917027
Max Magnitude0
ClinVar
Risk rs58917027(C,G;C,G)
Alt rs58917027(C,G;C,G)
Reference rs58917027(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156100499A>C; NC_000001.10:g.156100499A>G
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041350.2, RCV000057407.1, RCV000208276.1,