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rs794728609

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728609(-;-)
Make rs794728609(-;G)
Make rs794728609(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156135937
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728609
ebirs794728609
HLIrs794728609
Exacrs794728609
Varsomers794728609
Maprs794728609
PheGenIrs794728609
hapmaprs794728609
1000 genomesrs794728609
hgdprs794728609
ensemblrs794728609
gopubmedrs794728609
geneviewrs794728609
scholarrs794728609
googlers794728609
pharmgkbrs794728609
gwascentralrs794728609
openSNPrs794728609
23andMers794728609
23andMe allrs794728609
SNP Nexus

SNPshotrs794728609
SNPdbers794728609
MSV3drs794728609
GWAS Ctlgrs794728609
Max Magnitude0
ClinVar
Risk rs794728609(G;G)
Alt rs794728609(G;G)
Reference rs794728609(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105728dupG
CLNSRC
CLNACC RCV000182390.1,