{{Rsnum
|rsid=137853021
|Chromosome=2
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SIX3
|position=44942443
|Gene_s=SIX3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=603714
|variant=0007
|rsnum=137853021
}}{{ClinVar
|rsid=137853021
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=45169582
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SIX3:6496; SIX3-AS1:100506108
|GENE_NAME=SIX3; SIX3-AS1
|GENE_ID=6496; 100506108
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.45169582G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603714.0007
|CLNSIG=5
|CLNCUI=C1834877
|CLNDBN=Holoprosencephaly 2
|Disease=Holoprosencephaly 2
|CLNACC=RCV000006472.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1834877:157170:2162
}}