{{Rsnum
|rsid=137852345
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=G6PD
|position=154532772
|Gene_s=G6PD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=305900
|variant=0051
|rsnum=137852345
}}{{ClinVar
|rsid=137852345
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=153760987
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=G6PD:2539
|GENE_NAME=G6PD
|GENE_ID=2539
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153760987G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000011153.2; RCV000074300.3
|CLNDBN=G6PD SERRES; ANEMIA, NONSEPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=305900.0051
|Disease=G6PD SERRES; ANEMIA
}}