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rs794728596

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728596(G;T)
Make rs794728596(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156137186
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728596
ebirs794728596
HLIrs794728596
Exacrs794728596
Varsomers794728596
Maprs794728596
PheGenIrs794728596
hapmaprs794728596
1000 genomesrs794728596
hgdprs794728596
ensemblrs794728596
gopubmedrs794728596
geneviewrs794728596
scholarrs794728596
googlers794728596
pharmgkbrs794728596
gwascentralrs794728596
openSNPrs794728596
23andMers794728596
23andMe allrs794728596
SNP Nexus

SNPshotrs794728596
SNPdbers794728596
MSV3drs794728596
GWAS Ctlgrs794728596
Max Magnitude0
ClinVar
Risk rs794728596(T;T)
Alt rs794728596(T;T)
Reference rs794728596(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106977G>T
CLNSRC
CLNACC RCV000182371.2,