Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728601

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728601(C;C)
Make rs794728601(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115097
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728601
ebirs794728601
HLIrs794728601
Exacrs794728601
Varsomers794728601
Maprs794728601
PheGenIrs794728601
hapmaprs794728601
1000 genomesrs794728601
hgdprs794728601
ensemblrs794728601
gopubmedrs794728601
geneviewrs794728601
scholarrs794728601
googlers794728601
pharmgkbrs794728601
gwascentralrs794728601
openSNPrs794728601
23andMers794728601
23andMe allrs794728601
SNP Nexus

SNPshotrs794728601
SNPdbers794728601
MSV3drs794728601
GWAS Ctlgrs794728601
Max Magnitude0
ClinVar
Risk rs794728601(C;C)
Alt rs794728601(C;C)
Reference rs794728601(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084888G>C
CLNSRC
CLNACC RCV000182381.2,