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rs794728599

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728599(G;G)
Make rs794728599(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156114982
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728599
ebirs794728599
HLIrs794728599
Exacrs794728599
Varsomers794728599
Maprs794728599
PheGenIrs794728599
hapmaprs794728599
1000 genomesrs794728599
hgdprs794728599
ensemblrs794728599
gopubmedrs794728599
geneviewrs794728599
scholarrs794728599
googlers794728599
pharmgkbrs794728599
gwascentralrs794728599
openSNPrs794728599
23andMers794728599
23andMe allrs794728599
SNP Nexus

SNPshotrs794728599
SNPdbers794728599
MSV3drs794728599
GWAS Ctlgrs794728599
Max Magnitude0
ClinVar
Risk rs794728599(G;G)
Alt rs794728599(G;G)
Reference rs794728599(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084773T>G
CLNSRC
CLNACC RCV000182379.1,