{{Rsnum
|rsid=193922649
|Chromosome=X
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=LAMP2
|position=120449063
|Gene_s=LAMP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922649
|Reversed=1
|FwdREF=A
|FwdALT=
|REF=CT
|ALT=C
|RSPOS=119582917
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.119582918delT
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy; Danon disease
|Disease=Primary familial hypertrophic cardiomyopathy; Danon disease
|Tags=RV;PM;OTHERKG;LSD
|CLNACC=RCV000030113.1; RCV000037418.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005; C0878677:300257:34587:419097006
|GENEINFO=LAMP2:3920
|GENE_ID=3920
|GENE_NAME=LAMP2
}}