{{Rsnum
|rsid=137852338
|Chromosome=X
|Orientation=minus
|geno1=(-;-)
|geno2=(-;ATC)
|geno3=(ATC;ATC)
|Gene=G6PD
|position=154546051
|Gene_s=G6PD,IKBKG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=305900
|variant=0041
|rsnum=137852338
}}{{ClinVar
|rsid=137852338
|Reversed=1
|FwdREF=TCA
|FwdALT=
|REF=TGAT
|ALT=T
|RSPOS=153774262
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=IKBKG:8517; G6PD:2539
|GENE_NAME=IKBKG; G6PD
|GENE_ID=8517; 2539
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153774266_153774268delGAT
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000011140.2; RCV000011141.2
|CLNDBN=G6PD SUNDERLAND; Anemia, nonspherocytic hemolytic, due to g6pd deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2720289:300908
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=305900.0041
|Disease=G6PD SUNDERLAND; Anemia
}}