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rs387906887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906887(C;T)
Make rs387906887(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position131039043
GeneLAMC3
is asnp
is mentioned by
dbSNPrs387906887
ebirs387906887
HLIrs387906887
Exacrs387906887
Varsomers387906887
Maprs387906887
PheGenIrs387906887
hapmaprs387906887
1000 genomesrs387906887
hgdprs387906887
ensemblrs387906887
gopubmedrs387906887
geneviewrs387906887
scholarrs387906887
googlers387906887
pharmgkbrs387906887
gwascentralrs387906887
openSNPrs387906887
23andMers387906887
23andMe allrs387906887
SNP Nexus

SNPshotrs387906887
SNPdbers387906887
MSV3drs387906887
GWAS Ctlgrs387906887
Max Magnitude0
ClinVar
Risk rs387906887(T;T)
Alt rs387906887(T;T)
Reference rs387906887(C;C)
Significance Pathogenic
Disease Cortical malformations
Variation info
Gene LAMC3
CLNDBN Cortical malformations, occipital
Reversed 0
HGVS NC_000009.11:g.133914430C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023371.2,