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rs60682848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs60682848(C;T)
Make rs60682848(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134838
GeneLMNA
is asnp
is mentioned by
dbSNPrs60682848
ebirs60682848
HLIrs60682848
Exacrs60682848
Varsomers60682848
Maprs60682848
PheGenIrs60682848
hapmaprs60682848
1000 genomesrs60682848
hgdprs60682848
ensemblrs60682848
gopubmedrs60682848
geneviewrs60682848
scholarrs60682848
googlers60682848
pharmgkbrs60682848
gwascentralrs60682848
openSNPrs60682848
23andMers60682848
23andMe allrs60682848
SNP Nexus

SNPshotrs60682848
SNPdbers60682848
MSV3drs60682848
GWAS Ctlgrs60682848
Max Magnitude0
ClinVar
Risk rs60682848(T;T)
Alt rs60682848(T;T)
Reference rs60682848(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1A not provided Limb-girdle muscular dystrophy Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Dilated cardiomyopathy 1A not provided Limb-girdle muscular dystrophy, type 1B Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104629C>T
CLNSRC ClinVar Epithelial Biology GeneReviews
CLNACC RCV000056001.4, RCV000057442.3, RCV000194831.1, RCV000211792.1,