{{Rsnum
|rsid=121434488
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PAFAH1B1
|position=2674110
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAFAH1B1
}}{{omim
|id=601545
|rsnum=121434488
|variant=0008
}}{{ClinVar
|rsid=121434488
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=2577404
|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.2577404G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601545.0008
|CLNSIG=5
|CLNCUI=C1848201
|CLNDBN=Subcortical band heterotopia
|Disease=Subcortical band heterotopia
|CLNACC=RCV000008547.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1848201
}}