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rs1064796677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position156136042
GeneLMNA
is asnp
is mentioned by
dbSNPrs1064796677
dbSNP (old)rs1064796677
ClinGenrs1064796677
ebirs1064796677
HLIrs1064796677
Exacrs1064796677
Gnomadrs1064796677
Varsomers1064796677
Maprs1064796677
PheGenIrs1064796677
Biobankrs1064796677
1000 genomesrs1064796677
hgdprs1064796677
ensemblrs1064796677
gopubmedrs1064796677
geneviewrs1064796677
scholarrs1064796677
googlers1064796677
pharmgkbrs1064796677
gwascentralrs1064796677
openSNPrs1064796677
23andMers1064796677
23andMe allrs1064796677
SNPshotrs1064796677
SNPdbers1064796677
MSV3drs1064796677
GWAS Ctlgrs1064796677
Max Magnitude0
ClinVar
Risk rs1064796677(T;T)
Alt rs1064796677(T;T)
Reference Rs1064796677(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105833C>T
CLNSRC
CLNACC RCV000481311.1,