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rs1064797095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome19
Position35126265
GeneLGI4
is asnp
is mentioned by
dbSNPrs1064797095
dbSNP (classic)rs1064797095
ClinGenrs1064797095
ebirs1064797095
HLIrs1064797095
Exacrs1064797095
Gnomadrs1064797095
Varsomers1064797095
LitVarrs1064797095
Maprs1064797095
PheGenIrs1064797095
Biobankrs1064797095
1000 genomesrs1064797095
hgdprs1064797095
ensemblrs1064797095
geneviewrs1064797095
scholarrs1064797095
googlers1064797095
pharmgkbrs1064797095
gwascentralrs1064797095
openSNPrs1064797095
23andMers1064797095
23andMe allrs1064797095
SNPshotrs1064797095
SNPdbers1064797095
MSV3drs1064797095
GWAS Ctlgrs1064797095
Max Magnitude0
ClinVar
Risk rs1064797095(T;T)
Alt rs1064797095(T;T)
Reference Rs1064797095(G;G)
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.35617169C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000487493.1,