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rs794728604

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728604(-;-)
Make rs794728604(-;T)
Make rs794728604(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115257
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728604
ebirs794728604
HLIrs794728604
Exacrs794728604
Varsomers794728604
Maprs794728604
PheGenIrs794728604
hapmaprs794728604
1000 genomesrs794728604
hgdprs794728604
ensemblrs794728604
gopubmedrs794728604
geneviewrs794728604
scholarrs794728604
googlers794728604
pharmgkbrs794728604
gwascentralrs794728604
openSNPrs794728604
23andMers794728604
23andMe allrs794728604
SNP Nexus

SNPshotrs794728604
SNPdbers794728604
MSV3drs794728604
GWAS Ctlgrs794728604
Max Magnitude0
ClinVar
Risk rs794728604(T;T)
Alt rs794728604(T;T)
Reference rs794728604(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156085048dupT
CLNSRC
CLNACC RCV000182385.1,