{{Rsnum
|rsid=267607202
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=KLF1
|position=12885368
|Gene_s=KLF1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000009566.3
|CLNALLE=1
|CLNDBN=HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, KLF1-RELATED
|CLNHGVS=NC_000019.9:g.12996182T>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600599.0005
|Disease=HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
|FwdALT=T
|FwdREF=A
|GENEINFO=KLF1:10661
|GENE_ID=10661
|GENE_NAME=KLF1
|REF=T
|RSPOS=12996182
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607202
}}