{{Rsnum
|rsid=121434489
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PAFAH1B1
|position=2638310
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAFAH1B1
}}{{omim
|id=601545
|rsnum=121434489
|variant=0009
}}{{ClinVar
|rsid=121434489
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2541604
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PAFAH1B1:5048
|GENE_NAME=PAFAH1B1
|GENE_ID=5048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.2541604C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601545.0009
|CLNSIG=5
|CLNCUI=C1848201; C1843916
|CLNDBN=Subcortical band heterotopia; Lissencephaly 1
|Disease=Subcortical band heterotopia; Lissencephaly 1
|CLNACC=RCV000008548.1; RCV000008549.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM
|CLNDSDBID=C1848201; NBK5189:C1843916:607432
}}