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rs1064794966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position156135211
GeneLMNA
is asnp
is mentioned by
dbSNPrs1064794966
dbSNP (classic)rs1064794966
ClinGenrs1064794966
ebirs1064794966
HLIrs1064794966
Exacrs1064794966
Gnomadrs1064794966
Varsomers1064794966
LitVarrs1064794966
Maprs1064794966
PheGenIrs1064794966
Biobankrs1064794966
1000 genomesrs1064794966
hgdprs1064794966
ensemblrs1064794966
geneviewrs1064794966
scholarrs1064794966
googlers1064794966
pharmgkbrs1064794966
gwascentralrs1064794966
openSNPrs1064794966
23andMers1064794966
23andMe allrs1064794966
SNPshotrs1064794966
SNPdbers1064794966
MSV3drs1064794966
GWAS Ctlgrs1064794966
Max Magnitude0
ClinVar
Risk rs1064794966(-;-)
Alt rs1064794966(-;-)
Reference Rs1064794966(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105002delG
CLNSRC
CLNACC RCV000483218.1,