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rs1064793882

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAAC;AGAAC) 0 common in clinvar
Chromosome1
Position156115082
GeneLMNA
is asnp
is mentioned by
dbSNPrs1064793882
dbSNP (old)rs1064793882
ClinGenrs1064793882
ebirs1064793882
HLIrs1064793882
Exacrs1064793882
Gnomadrs1064793882
Varsomers1064793882
Maprs1064793882
PheGenIrs1064793882
Biobankrs1064793882
1000 genomesrs1064793882
hgdprs1064793882
ensemblrs1064793882
gopubmedrs1064793882
geneviewrs1064793882
scholarrs1064793882
googlers1064793882
pharmgkbrs1064793882
gwascentralrs1064793882
openSNPrs1064793882
23andMers1064793882
23andMe allrs1064793882
SNPshotrs1064793882
SNPdbers1064793882
MSV3drs1064793882
GWAS Ctlgrs1064793882
Max Magnitude0
ClinVar
Risk rs1064793882(TCT;TCT)
Alt rs1064793882(TCT;TCT)
Reference Rs1064793882(AGAAC;AGAAC)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084873_156084877delAGAACinsTCT
CLNSRC
CLNACC RCV000486297.1,