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rs730880132

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880132(C;C)
Make rs730880132(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134875
GeneLMNA
is asnp
is mentioned by
dbSNPrs730880132
ebirs730880132
HLIrs730880132
Exacrs730880132
Varsomers730880132
Maprs730880132
PheGenIrs730880132
hapmaprs730880132
1000 genomesrs730880132
hgdprs730880132
ensemblrs730880132
gopubmedrs730880132
geneviewrs730880132
scholarrs730880132
googlers730880132
pharmgkbrs730880132
gwascentralrs730880132
openSNPrs730880132
23andMers730880132
23andMe allrs730880132
SNP Nexus

SNPshotrs730880132
SNPdbers730880132
MSV3drs730880132
GWAS Ctlgrs730880132
Max Magnitude0
ClinVar
Risk rs730880132(C;C)
Alt rs730880132(C;C)
Reference rs730880132(T;T)
Significance Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104666T>C
CLNSRC
CLNACC RCV000157292.1,