{{Rsnum
|rsid=104893767
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PROK2
|position=71784959
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PROK2
}}{{omim
|id=607002
|rsnum=104893767
|variant=0001
}}{{ClinVar
|rsid=104893767
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=71834110
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PROK2:60675
|GENE_NAME=PROK2
|GENE_ID=60675
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.71834110C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607002.0001
|CLNSIG=5
|CLNCUI=C1857720
|CLNDBN=Kallmann syndrome 4
|Disease=Kallmann syndrome 4
|CLNACC=RCV000003784.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C1857720:610628:478
}}