{{Rsnum
|rsid=41297018
|Gene=DCLRE1C
|Chromosome=10
|position=14935470
|Orientation=plus
|GMAF=0.009642
|Gene_s=DCLRE1C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=41297018
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=14977469
|CHROM=10
|GMAF=0.0096
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x05006800000004051e100100
|GENEINFO=DCLRE1C:64421
|GENE_NAME=DCLRE1C
|GENE_ID=64421
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.14977469C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Severe combined immunodeficiency disease
|Disease=Severe combined immunodeficiency disease
|Tags=RV;PM;PMC;VLD;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD
|CAF=0.9904; 0.009642
|CLNACC=RCV000029656.1
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0085110:31323000
|COMMON=1
}}

{{PMID Auto
|PMID=18223550
|Title=Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients.
}}

{{PMID Auto
|PMID=19953608
|Title=The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.
}}

{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}