{{Rsnum
|rsid=267606693
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=WDPCP
|position=63487491
|Gene_s=WDPCP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000000064.1
|CLNALLE=1
|CLNDBN=Meckel syndrome, type 6, modifier of
|CLNHGVS=NC_000002.11:g.63714625C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613580.0003
|Disease=Meckel syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=WDPCP:51057
|GENE_ID=51057
|GENE_NAME=WDPCP
|REF=C
|RSPOS=63714625
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606693
}}