{{Rsnum
|rsid=267606783
|Chromosome=9
|position=127854354
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ENG
|Gene_s=ENG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNACC=RCV000018153.26
|CLNALLE=1
|CLNDBN=Hereditary hemorrhagic telangiectasia type 1
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1351:CN034812:187300:21877004
|CLNHGVS=NC_000009.11:g.130616633A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131195.0006
|Disease=Hereditary hemorrhagic telangiectasia type 1
|FwdALT=C
|FwdREF=T
|GENEINFO=ENG:2022
|GENE_ID=2022
|GENE_NAME=ENG
|REF=A
|RSPOS=130616633
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606783
}}