{{Rsnum
|rsid=281865142
|Chromosome=11
|position=111908949
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=CRYAB
|Gene_s=CRYAB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000032215.1
|CLNALLE=1
|CLNDBN=Alpha-B crystallinopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=NBK1499:C1837317:608810:613869:280553
|CLNHGVS=NC_000011.9:g.111779673delA
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1499
|Disease=Alpha-B crystallinopathy
|FwdREF=T
|REF=GA
|RSPOS=111779672
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281865142
|GENEINFO=CRYAB:1410
|GENE_ID=1410
|GENE_NAME=CRYAB
}}{{PMID Auto
|PMID=21130652
|Title=Infantile onset myofibrillar myopathy due to recessive CRYAB mutations.
}}