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rs794728610

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs794728610(-;-)
Make rs794728610(-;AC)
Make rs794728610(AC;AC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156135942
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728610
ebirs794728610
HLIrs794728610
Exacrs794728610
Varsomers794728610
Maprs794728610
PheGenIrs794728610
hapmaprs794728610
1000 genomesrs794728610
hgdprs794728610
ensemblrs794728610
gopubmedrs794728610
geneviewrs794728610
scholarrs794728610
googlers794728610
pharmgkbrs794728610
gwascentralrs794728610
openSNPrs794728610
23andMers794728610
23andMe allrs794728610
SNP Nexus

SNPshotrs794728610
SNPdbers794728610
MSV3drs794728610
GWAS Ctlgrs794728610
Max Magnitude0
ClinVar
Risk rs794728610(;)
Alt rs794728610(;)
Reference rs794728610(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105733_156105734delAC
CLNSRC
CLNACC RCV000182391.2,