{{Rsnum
|rsid=137853084
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SALL1
|position=51140966
|Gene_s=SALL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602218
|variant=0010
|rsnum=137853084
}}{{ClinVar
|rsid=137853084
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=51174877
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SALL1:6299
|GENE_NAME=SALL1
|GENE_ID=6299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.51174877A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602218.0010
|CLNSIG=5
|CLNCUI=C0265246; C0265240
|CLNDBN=Townes syndrome; Goldenhar syndrome
|Disease=Townes syndrome; Goldenhar syndrome
|CLNACC=RCV000007860.2; RCV000007861.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1445:C0265246:107480:C1862683:857:24750000; NBK5199:C0265240:164210:374:109393007:15557005:205418005:367462009
}}