{{Rsnum
|rsid=74315419
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PROKR2
|position=5302226
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PROKR2
}}{{omim
|id=607123
|rsnum=74315419
|variant=0005
}}{{ClinVar
|rsid=74315419
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5282872
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PROKR2:128674
|GENE_NAME=PROKR2
|GENE_ID=128674
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.5282872C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=607123.0005
|CLNSIG=5
|CLNCUI=C2930927
|CLNDBN=Kallmann syndrome 3
|Disease=Kallmann syndrome 3
|CLNACC=RCV000022410.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C2930927:244200:478
}}