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rs794728607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACAGGCTGCAG;ACAGGCTGCAG) 0 common in clinvar
Make rs794728607(-;-)
Make rs794728607(-;AGGCTGCAGAC)
Make rs794728607(AGGCTGCAGAC;AGGCTGCAGAC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134475
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728607
dbSNP (old)rs794728607
ClinGenrs794728607
ebirs794728607
HLIrs794728607
Exacrs794728607
Gnomadrs794728607
Varsomers794728607
Maprs794728607
PheGenIrs794728607
Biobankrs794728607
1000 genomesrs794728607
hgdprs794728607
ensemblrs794728607
gopubmedrs794728607
geneviewrs794728607
scholarrs794728607
googlers794728607
pharmgkbrs794728607
gwascentralrs794728607
openSNPrs794728607
23andMers794728607
23andMe allrs794728607
SNP Nexus

SNPshotrs794728607
SNPdbers794728607
MSV3drs794728607
GWAS Ctlgrs794728607
Max Magnitude0
ClinVar
Risk rs794728607(-;-)
Alt rs794728607(-;-)
Reference Rs794728607(ACAGGCTGCAG;ACAGGCTGCAG)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104266_156104276delAGGCTGCAGAC
CLNSRC
CLNACC RCV000182388.1,