{{Rsnum
|rsid=121908156
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DCLRE1C
|position=14945110
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCLRE1C
}}{{omim
|id=605988
|rsnum=121908156
|variant=0001
}}{{ClinVar
|rsid=121908156
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=14987109
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DCLRE1C:64421
|GENE_NAME=DCLRE1C
|GENE_ID=64421
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.14987109G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605988.0001
|CLNSIG=5
|CLNCUI=C1865370
|CLNDBN=Severe combined immunodeficiency with sensitivity to ionizing radiation
|Disease=Severe combined immunodeficiency with sensitivity to ionizing radiation
|CLNACC=RCV000004929.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1865370:602450:275
}}