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rs794728613

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728613(A;A)
Make rs794728613(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156136941
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728613
ebirs794728613
HLIrs794728613
Exacrs794728613
Varsomers794728613
Maprs794728613
PheGenIrs794728613
hapmaprs794728613
1000 genomesrs794728613
hgdprs794728613
ensemblrs794728613
gopubmedrs794728613
geneviewrs794728613
scholarrs794728613
googlers794728613
pharmgkbrs794728613
gwascentralrs794728613
openSNPrs794728613
23andMers794728613
23andMe allrs794728613
SNP Nexus

SNPshotrs794728613
SNPdbers794728613
MSV3drs794728613
GWAS Ctlgrs794728613
Max Magnitude0
ClinVar
Risk rs794728613(A;A)
Alt rs794728613(A;A)
Reference rs794728613(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106732G>A
CLNSRC
CLNACC RCV000182396.2,