Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064797094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome19
Position35125506
GeneLGI4
is asnp
is mentioned by
dbSNPrs1064797094
dbSNP (old)rs1064797094
ClinGenrs1064797094
ebirs1064797094
HLIrs1064797094
Exacrs1064797094
Gnomadrs1064797094
Varsomers1064797094
Maprs1064797094
PheGenIrs1064797094
Biobankrs1064797094
1000 genomesrs1064797094
hgdprs1064797094
ensemblrs1064797094
gopubmedrs1064797094
geneviewrs1064797094
scholarrs1064797094
googlers1064797094
pharmgkbrs1064797094
gwascentralrs1064797094
openSNPrs1064797094
23andMers1064797094
23andMe allrs1064797094
SNPshotrs1064797094
SNPdbers1064797094
MSV3drs1064797094
GWAS Ctlgrs1064797094
Max Magnitude0
ClinVar
Risk rs1064797094(A;A)
Alt rs1064797094(A;A)
Reference Rs1064797094(T;T)
Significance Pathogenic
Disease Arthrogryposis multiplex congenita
Variation info
Gene LGI4
CLNDBN Arthrogryposis multiplex congenita, neurogenic, with myelin defect
Reversed 1
HGVS NC_000019.9:g.35616410A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000487490.1,