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rs60446065

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs60446065(A;A)
Make rs60446065(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156115045
GeneLMNA
is asnp
is mentioned by
dbSNPrs60446065
ebirs60446065
HLIrs60446065
Exacrs60446065
Varsomers60446065
Maprs60446065
PheGenIrs60446065
hapmaprs60446065
1000 genomesrs60446065
hgdprs60446065
ensemblrs60446065
gopubmedrs60446065
geneviewrs60446065
scholarrs60446065
googlers60446065
pharmgkbrs60446065
gwascentralrs60446065
openSNPrs60446065
23andMers60446065
23andMe allrs60446065
SNP Nexus

SNPshotrs60446065
SNPdbers60446065
MSV3drs60446065
GWAS Ctlgrs60446065
Max Magnitude0
ClinVar
Risk rs60446065(A;A)
Alt rs60446065(A;A)
Reference rs60446065(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084836G>A
CLNSRC
CLNACC RCV000057262.2,