{{Rsnum
|rsid=104894827
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GLA
|position=101398033
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLA,RPL36A-HNRNPH2
}}{{omim
|id=300644
|rsnum=104894827
|variant=0001
}}{{ClinVar
|rsid=104894827
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=100653021
|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=1
|CLNHGVS=NC_000023.10:g.100653021G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300644.0001
|CLNSIG=5
|CLNCUI=C0002986
|CLNDBN=Fabry's disease; AllHighlyPenetrant
|Disease=Fabry's disease; AllHighlyPenetrant
|CLNACC=RCV000011459.1; RCV000035299.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1292:C0002986:301500:324:16652001; CN169374
}}