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rs794728594

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728594(A;A)
Make rs794728594(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156135247
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728594
ebirs794728594
HLIrs794728594
Exacrs794728594
Varsomers794728594
Maprs794728594
PheGenIrs794728594
hapmaprs794728594
1000 genomesrs794728594
hgdprs794728594
ensemblrs794728594
gopubmedrs794728594
geneviewrs794728594
scholarrs794728594
googlers794728594
pharmgkbrs794728594
gwascentralrs794728594
openSNPrs794728594
23andMers794728594
23andMe allrs794728594
SNP Nexus

SNPshotrs794728594
SNPdbers794728594
MSV3drs794728594
GWAS Ctlgrs794728594
Max Magnitude0
ClinVar
Risk rs794728594(A;A)
Alt rs794728594(A;A)
Reference rs794728594(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105038G>A
CLNSRC
CLNACC RCV000182365.2,