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rs794728602

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728602(A;A)
Make rs794728602(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115168
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728602
ebirs794728602
HLIrs794728602
Exacrs794728602
Varsomers794728602
Maprs794728602
PheGenIrs794728602
hapmaprs794728602
1000 genomesrs794728602
hgdprs794728602
ensemblrs794728602
gopubmedrs794728602
geneviewrs794728602
scholarrs794728602
googlers794728602
pharmgkbrs794728602
gwascentralrs794728602
openSNPrs794728602
23andMers794728602
23andMe allrs794728602
SNP Nexus

SNPshotrs794728602
SNPdbers794728602
MSV3drs794728602
GWAS Ctlgrs794728602
Max Magnitude0
ClinVar
Risk rs794728602(A;A)
Alt rs794728602(A;A)
Reference rs794728602(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084959G>A
CLNSRC
CLNACC RCV000182383.1,