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rs794728606

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728606(-;-)
Make rs794728606(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134411
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728606
ebirs794728606
HLIrs794728606
Exacrs794728606
Varsomers794728606
Maprs794728606
PheGenIrs794728606
hapmaprs794728606
1000 genomesrs794728606
hgdprs794728606
ensemblrs794728606
gopubmedrs794728606
geneviewrs794728606
scholarrs794728606
googlers794728606
pharmgkbrs794728606
gwascentralrs794728606
openSNPrs794728606
23andMers794728606
23andMe allrs794728606
SNP Nexus

SNPshotrs794728606
SNPdbers794728606
MSV3drs794728606
GWAS Ctlgrs794728606
Max Magnitude0
ClinVar
Risk rs794728606(;)
Alt rs794728606(;)
Reference rs794728606(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104202delA
CLNSRC
CLNACC RCV000182387.2,