{{Rsnum
|rsid=80359890
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SH3TC2
|position=149042718
|Gene_s=SH3TC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80359890
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=148422281
|CHROM=5
|dbSNPBuildID=134
|SSR=0
|SAO=0
|VP=0x050160000000040002110100
|GENEINFO=SH3TC2:79628
|GENE_NAME=SH3TC2
|GENE_ID=79628
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.148422281A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1468; 608206.0008
|CLNSIG=5
|CLNCUI=C1866636; C3150596
|CLNDBN=Charcot-Marie-Tooth disease, type 4C; Mononeuropathy of the median nerve, mild
|Disease=Charcot-Marie-Tooth disease; Mononeuropathy of the median nerve
|CLNACC=RCV000002590.1; RCV000002591.1
|Tags=PM;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=NBK1340:NBK1468:C1866636:601596:99949; C3150596:613353
}}