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rs794728590

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728590(A;T)
Make rs794728590(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134448
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728590
ebirs794728590
HLIrs794728590
Exacrs794728590
Varsomers794728590
Maprs794728590
PheGenIrs794728590
hapmaprs794728590
1000 genomesrs794728590
hgdprs794728590
ensemblrs794728590
gopubmedrs794728590
geneviewrs794728590
scholarrs794728590
googlers794728590
pharmgkbrs794728590
gwascentralrs794728590
openSNPrs794728590
23andMers794728590
23andMe allrs794728590
SNP Nexus

SNPshotrs794728590
SNPdbers794728590
MSV3drs794728590
GWAS Ctlgrs794728590
Max Magnitude0
ClinVar
Risk rs794728590(T;T)
Alt rs794728590(T;T)
Reference rs794728590(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104239A>T
CLNSRC
CLNACC RCV000182359.1,