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rs61295588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61295588(C;C)
Make rs61295588(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134809
GeneLMNA
is asnp
is mentioned by
dbSNPrs61295588
ebirs61295588
HLIrs61295588
Exacrs61295588
Varsomers61295588
Maprs61295588
PheGenIrs61295588
hapmaprs61295588
1000 genomesrs61295588
hgdprs61295588
ensemblrs61295588
gopubmedrs61295588
geneviewrs61295588
scholarrs61295588
googlers61295588
pharmgkbrs61295588
gwascentralrs61295588
openSNPrs61295588
23andMers61295588
23andMe allrs61295588
SNP Nexus

SNPshotrs61295588
SNPdbers61295588
MSV3drs61295588
GWAS Ctlgrs61295588
Max Magnitude0
ClinVar
Risk rs61295588(C;C)
Alt rs61295588(C;C)
Reference rs61295588(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 1A not provided
Variation info
Gene LMNA
CLNDBN Dilated cardiomyopathy 1A not provided
Reversed 0
HGVS NC_000001.10:g.156104600T>C
CLNSRC ClinVar Epithelial Biology GeneReviews
CLNACC RCV000056000.1, RCV000057438.1,