{{Rsnum
|rsid=387907355
|Chromosome=12
|position=48980630
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=WNT1
|Gene_s=WNT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000043494.25
|CLNALLE=1
|CLNDBN=Osteogenesis imperfecta type 15
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN169385:615220:666
|CLNHGVS=NC_000012.11:g.49374413G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164820.0003
|Disease=Osteogenesis imperfecta type 15
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=49374413
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907355
|GENEINFO=WNT1:7471
|GENE_ID=7471
|GENE_NAME=WNT1
}}