{{Rsnum
|rsid=137853006
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PROM1
|position=16013299
|Gene_s=PROM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=604365
|variant=0003
|rsnum=137853006
}}{{ClinVar
|rsid=137853006
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=16014922
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PROM1:8842
|GENE_NAME=PROM1
|GENE_ID=8842
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.16014922G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604365.0003
|CLNSIG=5
|CLNCUI=C1863534; C0339512; C2675210
|CLNDBN=Stargardt disease 4; Bull's eye macular dystrophy; Cone-rod dystrophy 12
|Disease=Stargardt disease 4; Bull's eye macular dystrophy; Cone-rod dystrophy 12
|CLNACC=RCV000005960.1; RCV000005961.1; RCV000005962.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1863534:603786:827; C0339512:608051:232050001; C2675210:612657:1872
}}