{{Rsnum
|rsid=149782619
|Gene=HINT1
|Chromosome=5
|position=131165096
|Orientation=plus
|GMAF=0.0004591
|Gene_s=HINT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G
|CAF=0.9995; 0.0004591
|CHROM=5
|CLNACC=RCV000030852.1
|CLNALLE=1
|CLNDBN=Gamstorp-Wohlfart syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074193:137200:324442
|CLNHGVS=NC_000005.9:g.130500789C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601314.0001
|COMMON=0
|Disease=Gamstorp-Wohlfart syndrome
|FwdALT=G
|FwdREF=C
|GENEINFO=HINT1:3094
|GENE_ID=3094
|GENE_NAME=HINT1
|REF=C
|RSPOS=130500789
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000040016110100
|WGT=0
|dbSNPBuildID=134
|rsid=149782619
}}