{{Rsnum
|rsid=104894859
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMP2
|position=120441862
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LAMP2
}}{{omim
|id=309060
|rsnum=104894859
|variant=0011
}}{{ClinVar
|rsid=104894859
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=119575717
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LAMP2:3920
|GENE_NAME=LAMP2
|GENE_ID=3920
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.119575717A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=309060.0011
|CLNSIG=5
|CLNCUI=C0878677
|CLNDBN=Danon disease
|Disease=Danon disease
|CLNACC=RCV000010664.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0878677:300257:34587:419097006
}}