{{Rsnum
|rsid=72549406
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FAM126A
|position=22977340
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FAM126A
}}{{omim
|id=610531
|rsnum=72549406
|variant=0002
}}

{{ClinVar
|rsid=72549406
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=23016959
|CHROM=7
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=FAM126A:84668
|GENE_NAME=FAM126A
|GENE_ID=84668
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.23016959C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2587; 610531.0002
|CLNSIG=5
|CLNCUI=C2674508; C2674508,.
|CLNDBN=Hypomyelination and Congenital Cataract
|Disease=Hypomyelination and Congenital Cataract
|CLNACC=RCV000001274.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2587:C2674508:610532:85163
}}

{{PMID Auto
|PMID=16951682
|Title=Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}