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rs794728603

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728603(-;-)
Make rs794728603(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156115247
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728603
ebirs794728603
HLIrs794728603
Exacrs794728603
Varsomers794728603
Maprs794728603
PheGenIrs794728603
hapmaprs794728603
1000 genomesrs794728603
hgdprs794728603
ensemblrs794728603
gopubmedrs794728603
geneviewrs794728603
scholarrs794728603
googlers794728603
pharmgkbrs794728603
gwascentralrs794728603
openSNPrs794728603
23andMers794728603
23andMe allrs794728603
SNP Nexus

SNPshotrs794728603
SNPdbers794728603
MSV3drs794728603
GWAS Ctlgrs794728603
Max Magnitude0
ClinVar
Risk rs794728603(;)
Alt rs794728603(;)
Reference rs794728603(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156085038delG
CLNSRC
CLNACC RCV000182384.1,