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rs794728595

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728595(A;A)
Make rs794728595(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156137184
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728595
ebirs794728595
HLIrs794728595
Exacrs794728595
Varsomers794728595
Maprs794728595
PheGenIrs794728595
hapmaprs794728595
1000 genomesrs794728595
hgdprs794728595
ensemblrs794728595
gopubmedrs794728595
geneviewrs794728595
scholarrs794728595
googlers794728595
pharmgkbrs794728595
gwascentralrs794728595
openSNPrs794728595
23andMers794728595
23andMe allrs794728595
SNP Nexus

SNPshotrs794728595
SNPdbers794728595
MSV3drs794728595
GWAS Ctlgrs794728595
Max Magnitude0
ClinVar
Risk rs794728595(A;A)
Alt rs794728595(A;A)
Reference rs794728595(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106975G>A
CLNSRC
CLNACC RCV000182370.2,