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rs794728611

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs794728611(-;-)
Make rs794728611(-;AG)
Make rs794728611(AG;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156136332
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728611
ebirs794728611
HLIrs794728611
Exacrs794728611
Varsomers794728611
Maprs794728611
PheGenIrs794728611
hapmaprs794728611
1000 genomesrs794728611
hgdprs794728611
ensemblrs794728611
gopubmedrs794728611
geneviewrs794728611
scholarrs794728611
googlers794728611
pharmgkbrs794728611
gwascentralrs794728611
openSNPrs794728611
23andMers794728611
23andMe allrs794728611
SNP Nexus

SNPshotrs794728611
SNPdbers794728611
MSV3drs794728611
GWAS Ctlgrs794728611
Max Magnitude0
ClinVar
Risk rs794728611(;)
Alt rs794728611(;)
Reference rs794728611(GA;GA)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106123_156106124delAG
CLNSRC
CLNACC RCV000182392.1,