{{Rsnum
|rsid=61734651
|Gene=COL9A3
|Chromosome=20
|position=62819980
|Orientation=plus
|GMAF=0.03076
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=COL9A3
}}{{omim
|id=120270
|rsnum=61734651
|variant=0003
}}

{{ClinVar
|rsid=61734651
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=61451332
|CHROM=20
|GMAF=0.0307
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050160000000150516110100
|GENEINFO=COL9A3:1299
|GENE_NAME=COL9A3
|GENE_ID=1299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.61451332C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9692; 0.03076
|CLNACC=RCV000018677.1
|CLNDBN=Intervertebral disc disease, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=120270.0003
|COMMON=1
|Disease=Intervertebral disc disease
}}

{{GET Evidence
|gene=COL9A3
|aa_change=Arg103Trp
|aa_change_short=R103W
|impact=pathogenic
|qualified_impact=Moderate clinical importance, Likely pathogenic
|inheritance=dominant
|quality_scores=Array
|dbsnp_id=rs61734651
|overall_frequency_n=517
|overall_frequency_d=10758
|overall_frequency=0.0480573
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|qualityscore_case_control=5
|qualitycomment_case_control=Y
|qualityscore_familial=0
|qualitycomment_familial=Y
|qualityscore_severity=3
|qualitycomment_severity=Y
|qualityscore_treatability=2
|qualitycomment_treatability=Y
|gene_in_genetests=Y
|in_omim=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=7
|autoscore=5
|webscore=N
|n_web_uneval=8
|variant_evidence=1
|clinical_importance=1
|summary_short=Carriers of this collagen variant are associated with having a significantly increased risk of lumbar disc disease (~11% total risk compared to a typical risk of 4%). 
}}

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