{{Rsnum
|rsid=104894535
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SALL1
|position=51141107
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SALL1
}}{{omim
|id=602218
|rsnum=104894535
|variant=0002
}}{{ClinVar
|rsid=104894535
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=51175018
|CHROM=16
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050060000000000002110100
|GENEINFO=SALL1:6299
|GENE_NAME=SALL1
|GENE_ID=6299
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.51175018G>C; NC_000016.9:g.51175018G>T
|CLNSRCID=
602218.0004; 602218.0002
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000007854.1; RCV000007852.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDBN=Townes syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1445:C0265246:107480:C1862683:857:24750000
|CLNSRC=OMIM Allelic Variant
|Disease=Townes syndrome
}}