{{Rsnum
|rsid=121918653
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KITLG
|position=88545774
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KITLG
}}{{omim
|id=184745
|rsnum=121918653
|variant=0003
}}{{ClinVar
|rsid=121918653
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=88939551
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KITLG:4254
|GENE_NAME=KITLG
|GENE_ID=4254
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.88939551T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=184745.0003
|CLNSIG=5
|CLNCUI=C1840392
|CLNDBN=Hyperpigmentation, familial progressive, 2
|Disease=Hyperpigmentation
|CLNACC=RCV000013661.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1840392:145250
}}