{{Rsnum
|rsid=397514492
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HINT1
|position=131162604
|Gene_s=HINT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=5
|CLNACC=RCV000030857.2
|CLNALLE=1
|CLNDBN=Gamstorp-Wohlfart syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074193:137200:324442
|CLNHGVS=NC_000005.9:g.130498297G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601314.0006
|Disease=Gamstorp-Wohlfart syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=HINT1:3094
|GENE_ID=3094
|GENE_NAME=HINT1
|REF=G
|RSPOS=130498297
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514492
}}