{{Rsnum
|rsid=104894828
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GLA
|position=101398467
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLA,RPL36A-HNRNPH2
}}{{omim
|id=300644
|rsnum=104894828
|variant=0003
}}{{ClinVar
|rsid=104894828
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=100653455
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RPL36A-HNRNPH2:100529097; GLA:2717
|GENE_NAME=RPL36A-HNRNPH2; GLA
|GENE_ID=100529097; 2717
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000023.10:g.100653455C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=881; 300644.0003
|CLNSIG=5
|CLNCUI=C1970820; C0002986
|CLNDBN=Fabry disease, cardiac variant; Fabry's disease; not provided
|Disease=Fabry disease; Fabry's disease; not provided
|CLNACC=RCV000011461.1; RCV000011462.1; RCV000078302.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1970820; NBK1292:C0002986:301500:324:16652001
}}