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rs1064797149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position93793200
GeneLGI1
is asnp
is mentioned by
dbSNPrs1064797149
dbSNP (old)rs1064797149
ClinGenrs1064797149
ebirs1064797149
HLIrs1064797149
Exacrs1064797149
Gnomadrs1064797149
Varsomers1064797149
Maprs1064797149
PheGenIrs1064797149
Biobankrs1064797149
1000 genomesrs1064797149
hgdprs1064797149
ensemblrs1064797149
gopubmedrs1064797149
geneviewrs1064797149
scholarrs1064797149
googlers1064797149
pharmgkbrs1064797149
gwascentralrs1064797149
openSNPrs1064797149
23andMers1064797149
23andMe allrs1064797149
SNPshotrs1064797149
SNPdbers1064797149
MSV3drs1064797149
GWAS Ctlgrs1064797149
Max Magnitude0
ClinVar
Risk rs1064797149(-;-)
Alt rs1064797149(-;-)
Reference Rs1064797149(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LGI1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.95552957delC
CLNSRC
CLNACC RCV000487910.1,