{{Rsnum
|rsid=387907167
|Chromosome=1
|position=9263569
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=H6PD
|Gene_s=H6PD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000024291.26
|CLNALLE=1
|CLNDBN=Deficiency of (R)-20-hydroxysteroid dehydrogenase
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1291245:604931:ORPHA168588:124138004
|CLNHGVS=NC_000001.11:g.9263569G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004285.3:c.1076G>A; 138090.0004
|Disease=Deficiency of (R)-20-hydroxysteroid dehydrogenase
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=9263569
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387907167
|GENEINFO=H6PD:9563
|GENE_ID=9563
|GENE_NAME=H6PD
|CLNORIGIN=1
}}