{{Rsnum
|rsid=387907327
|Chromosome=3
|position=142497116
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ATR
|Gene_s=ATR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=3
|CLNACC=RCV000034827.2
|CLNALLE=1
|CLNDBN=Seckel syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265202:210600:808:57917004
|CLNHGVS=NC_000003.11:g.142215958C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601215.0003
|Disease=Seckel syndrome
|FwdALT=T
|FwdREF=G
|REF=C
|RSPOS=142215958
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907327
|GENEINFO=ATR:545
|GENE_ID=545
|GENE_NAME=ATR
}}