{{Rsnum
|rsid=199823175
|Chromosome=2
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SIX3
|position=44942213
|Gene_s=SIX3,SIX3-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000023330.1; RCV000023331.1
|CLNALLE=1
|CLNDBN=Holoprosencephaly 2; Schizencephaly
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1530:C1834877:157170:2162; C0266484:269160:799:253159001
|CLNHGVS=NC_000002.11:g.45169352G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603714.0009
|Disease=Holoprosencephaly 2; Schizencephaly
|FwdALT=T
|FwdREF=G
|GENEINFO=SIX3:6496; SIX3-AS1:100506108
|GENE_ID=6496; 100506108
|GENE_NAME=SIX3; SIX3-AS1
|REF=G
|RSPOS=45169352
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=199823175
}}