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rs1064797093

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome19
Position35126848
GeneLGI4
is asnp
is mentioned by
dbSNPrs1064797093
dbSNP (old)rs1064797093
ClinGenrs1064797093
ebirs1064797093
HLIrs1064797093
Exacrs1064797093
Gnomadrs1064797093
Varsomers1064797093
Maprs1064797093
PheGenIrs1064797093
Biobankrs1064797093
1000 genomesrs1064797093
hgdprs1064797093
ensemblrs1064797093
gopubmedrs1064797093
geneviewrs1064797093
scholarrs1064797093
googlers1064797093
pharmgkbrs1064797093
gwascentralrs1064797093
openSNPrs1064797093
23andMers1064797093
23andMe allrs1064797093
SNPshotrs1064797093
SNPdbers1064797093
MSV3drs1064797093
GWAS Ctlgrs1064797093
Max Magnitude0
ClinVar
Risk rs1064797093(C;C)
Alt rs1064797093(C;C)
Reference Rs1064797093(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.35617752C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000487486.1,