{{Rsnum
|rsid=74315314
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GJC2
|position=228158572
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GJC2
}}{{omim
|id=608803
|rsnum=74315314
|variant=0005
}}{{ClinVar
|rsid=74315314
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=228158572
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=GJC2:57165
|GENE_NAME=GJC2
|GENE_ID=57165
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.228158572T>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_020435.3:c.814T>G; 608803.0005
|CLNSIG=5
|CLNCUI=C1837355
|CLNDBN=Leukodystrophy, hypomyelinating, 2
|Disease=Leukodystrophy
|CLNACC=RCV000002156.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1837355:608804:ORPHA280282
}}