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rs794728588

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728588(A;T)
Make rs794728588(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115262
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728588
ebirs794728588
HLIrs794728588
Exacrs794728588
Varsomers794728588
Maprs794728588
PheGenIrs794728588
hapmaprs794728588
1000 genomesrs794728588
hgdprs794728588
ensemblrs794728588
gopubmedrs794728588
geneviewrs794728588
scholarrs794728588
googlers794728588
pharmgkbrs794728588
gwascentralrs794728588
openSNPrs794728588
23andMers794728588
23andMe allrs794728588
SNP Nexus

SNPshotrs794728588
SNPdbers794728588
MSV3drs794728588
GWAS Ctlgrs794728588
Max Magnitude0
ClinVar
Risk rs794728588(T;T)
Alt rs794728588(T;T)
Reference rs794728588(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene LMNA
CLNDBN not provided not specified
Reversed 0
HGVS NC_000001.10:g.156085053A>T
CLNSRC
CLNACC RCV000182354.1, RCV000223737.1,