{{Rsnum
|rsid=36094464
|Gene=DSPP
|Chromosome=4
|position=87612388
|Orientation=plus
|GMAF=0.1088
|Gene_s=DSPP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=36094464
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=88533540
|CHROM=4
|GMAF=0.1085
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x05016800000015051e110100
|GENEINFO=DSPP:1834
|GENE_NAME=DSPP
|GENE_ID=1834
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.88533540A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=125485.0006
|CLNSIG=5
|CLNCUI=C0205730
|CLNDBN=Dentinogenesis imperfecta - Shield's type II
|Disease=Dentinogenesis imperfecta - Shield's type II
|CLNACC=RCV000018354.26
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.8912; 0.1088
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0205730:125490:166260:234969005
|COMMON=1
}}

{{PMID|18797159|OA=1
}} Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families.

{{GET Evidence
|gene=DSPP
|aa_change=Arg68Trp
|aa_change_short=R68W
|impact=benign
|qualified_impact=Low clinical importance, Uncertain benign
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs36094464
|overall_frequency_n=1413
|overall_frequency_d=9878
|overall_frequency=0.143045
|n_genomes=16
|n_genomes_annotated=0
|n_haplomes=18
|n_articles=3
|n_articles_annotated=3
|qualityscore_in_silico=!
|qualitycomment_in_silico=Y
|qualityscore_case_control=3
|qualitycomment_case_control=Y
|in_omim=Y
|nblosum100=7
|autoscore=2
|webscore=N
|variant_evidence=0
|clinical_importance=0
|summary_short=Probably benign. One report linked this to causing dentinogenesis Imperfecta type II in a large Swedish family, but subsequent publications have observed this is a common variant and conclude it is a nonpathogenic polymorphism.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}