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rs794728586

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728586(C;C)
Make rs794728586(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115170
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728586
ebirs794728586
HLIrs794728586
Exacrs794728586
Varsomers794728586
Maprs794728586
PheGenIrs794728586
hapmaprs794728586
1000 genomesrs794728586
hgdprs794728586
ensemblrs794728586
gopubmedrs794728586
geneviewrs794728586
scholarrs794728586
googlers794728586
pharmgkbrs794728586
gwascentralrs794728586
openSNPrs794728586
23andMers794728586
23andMe allrs794728586
SNP Nexus

SNPshotrs794728586
SNPdbers794728586
MSV3drs794728586
GWAS Ctlgrs794728586
Max Magnitude0
ClinVar
Risk rs794728586(C;C)
Alt rs794728586(C;C)
Reference rs794728586(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084961G>C
CLNSRC
CLNACC RCV000182351.1,