{{Rsnum
|rsid = 7252299
|geno1 = (A;A)
|geno2 = (A;C)
|geno3 = (C;C)
|Gene = ADAMTS10
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|Chromosome=19
|position=8580902
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS10
}}{{Venter SNP
|rsid=7252299
|allele=C
|frequency=
|uid=1103691086089
|type=homozygous_SNP
|hugo=ADAMTS10
|ensembl gene=ENSG00000142303
|ensembl transcript=ENST00000270328
|sift=
|disease=Defects in ADAMTS10 are a cause of the autosomal recessive form of Weill-Marchesani syndrome (WMS) (MIM:277600). WMS is characterized by the association of short stature, brachydactyly, joint stiffness, eye anomalies, including microspherophakia, ectopia of the lenses, severe myopia, and glaucoma; and, occasionally, heart defects.
}}

{{GET Evidence
|gene=ADAMTS10
|aa_change=His1101Gln
|aa_change_short=H1101Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7252299
|overall_frequency_n=10756
|overall_frequency_d=10758
|overall_frequency=0.999814
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=106
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-1
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}