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rs794728587

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728587(A;T)
Make rs794728587(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115253
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728587
ebirs794728587
HLIrs794728587
Exacrs794728587
Varsomers794728587
Maprs794728587
PheGenIrs794728587
hapmaprs794728587
1000 genomesrs794728587
hgdprs794728587
ensemblrs794728587
gopubmedrs794728587
geneviewrs794728587
scholarrs794728587
googlers794728587
pharmgkbrs794728587
gwascentralrs794728587
openSNPrs794728587
23andMers794728587
23andMe allrs794728587
SNP Nexus

SNPshotrs794728587
SNPdbers794728587
MSV3drs794728587
GWAS Ctlgrs794728587
Max Magnitude0
ClinVar
Risk rs794728587(T;T)
Alt rs794728587(T;T)
Reference rs794728587(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156085044A>T
CLNSRC
CLNACC RCV000182353.2,