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rs1064796394

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position156138608
GeneLMNA
is asnp
is mentioned by
dbSNPrs1064796394
dbSNP (old)rs1064796394
ClinGenrs1064796394
ebirs1064796394
HLIrs1064796394
Exacrs1064796394
Gnomadrs1064796394
Varsomers1064796394
Maprs1064796394
PheGenIrs1064796394
Biobankrs1064796394
1000 genomesrs1064796394
hgdprs1064796394
ensemblrs1064796394
gopubmedrs1064796394
geneviewrs1064796394
scholarrs1064796394
googlers1064796394
pharmgkbrs1064796394
gwascentralrs1064796394
openSNPrs1064796394
23andMers1064796394
23andMe allrs1064796394
SNPshotrs1064796394
SNPdbers1064796394
MSV3drs1064796394
GWAS Ctlgrs1064796394
Max Magnitude0
ClinVar
Risk rs1064796394(-;-)
Alt rs1064796394(-;-)
Reference Rs1064796394(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156108399delG
CLNSRC
CLNACC RCV000486027.1,