{{Rsnum
|rsid=137852513
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KAL1
|position=8585354
|Gene_s=KAL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308700
|variant=0003
|rsnum=137852513
}}{{ClinVar
|rsid=137852513
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=8553395
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KAL1:3730
|GENE_NAME=KAL1
|GENE_ID=3730
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.8553395G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300836.0003
|CLNSIG=5
|CLNCUI=CN035016
|CLNDBN=Kallmann syndrome 1
|Disease=Kallmann syndrome 1
|CLNACC=RCV000010687.4
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C1563719:308700:478
}}