{{Rsnum
|rsid=72552292
|Gene=GPD1L
|Chromosome=3
|position=32138608
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GPD1L
}}{{omim
|id=611778
|rsnum=72552292
|variant=0002
}}{{ClinVar
|rsid=72552292
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=32180100
|CHROM=3
|GMAF=0.0005
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050268000000000016110100
|GENEINFO=GPD1L:23171
|GENE_NAME=GPD1L
|GENE_ID=23171
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.32180100G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=611778.0002
|CLNSIG=5
|CLNCUI=C2673193
|CLNDBN=Brugada syndrome 2
|Disease=Brugada syndrome 2
|CLNACC=RCV000000823.1
|Tags=PM;PMC;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1517:C2673193:611777:130
|COMMON=0
}}{{PMID Auto
|PMID=17967976
|Title=Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.
|OA=1
}}