{{Rsnum
|rsid=387906887
|Chromosome=9
|position=131039043
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMC3
|Gene_s=LAMC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000023371.1
|CLNALLE=1
|CLNDBN=Cortical malformations, occipital
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3279875:614115:280640
|CLNHGVS=NC_000009.11:g.133914430C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604349.0003
|Disease=Cortical malformations
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=133914430
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906887
|GENEINFO=LAMC3:10319
|GENE_ID=10319
|GENE_NAME=LAMC3
}}