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rs794728612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs794728612(CG;TC)
Make rs794728612(TC;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156137756
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728612
dbSNP (old)rs794728612
ClinGenrs794728612
ebirs794728612
HLIrs794728612
Exacrs794728612
Gnomadrs794728612
Varsomers794728612
Maprs794728612
PheGenIrs794728612
Biobankrs794728612
1000 genomesrs794728612
hgdprs794728612
ensemblrs794728612
gopubmedrs794728612
geneviewrs794728612
scholarrs794728612
googlers794728612
pharmgkbrs794728612
gwascentralrs794728612
openSNPrs794728612
23andMers794728612
23andMe allrs794728612
SNP Nexus

SNPshotrs794728612
SNPdbers794728612
MSV3drs794728612
GWAS Ctlgrs794728612
Max Magnitude0
ClinVar
Risk rs794728612(TC;TC)
Alt rs794728612(TC;TC)
Reference Rs794728612(CG;CG)
Significance Pathogenic
Disease not provided Cardiovascular phenotype not specified
Variation info
Gene LMNA
CLNDBN not provided Cardiovascular phenotype not specified
Reversed 0
HGVS NC_000001.10:g.156107547_156107548delCGinsTC
CLNSRC
CLNACC RCV000182393.1, RCV000249124.1, RCV000362173.1,