{{Rsnum
|rsid=104894232
|Gene=HYLS1
|Chromosome=11
|position=125900000
|Orientation=plus
|GMAF=0.001377
|Gene_s=HYLS1,PUS3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=610693
|rsnum=104894232
|variant=0001
}}{{ClinVar
|rsid=104894232
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=125769895
|CHROM=11
|GMAF=0.0014
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=HYLS1:219844; PUS3:83480
|GENE_NAME=HYLS1; PUS3
|GENE_ID=219844; 83480
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.125769895A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000001202.1
|CLNDBN=Hydrolethalus syndrome
|CLNDSDB=MedGen
|CLNDSDBID=C2931104
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610693.0001
|COMMON=1
|Disease=Hydrolethalus syndrome
}}