{{Rsnum
|rsid=121912987
|Chromosome=4
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=DSPP
|position=87612105
|Gene_s=DSPP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=125485
|rsnum=121912987
|variant=0004
}}{{ClinVar
|rsid=121912987
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=88533257
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DSPP:1834
|GENE_NAME=DSPP
|GENE_ID=1834
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.88533257G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=125485.0004
|CLNSIG=5
|CLNCUI=C0205730; C0399378
|CLNDBN=Deafness, autosomal dominant nonsyndromic sensorineural 39, with dentinogenesis imperfecta 1; Dentinogenesis imperfecta - Shield's type II; Dentinogenesis imperfecta - Shield's type III
|Disease=Deafness; Dentinogenesis imperfecta - Shield's type II; Dentinogenesis imperfecta - Shield's type III
|CLNACC=RCV000018350.27; RCV000018351.27; RCV000018352.27
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0205730:125490:166260:234969005; C0399378:125500:166265:234970006
}}