{{Rsnum
|rsid=104894845
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GLA
|position=101401752
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GLA,RPL36A-HNRNPH2
}}{{omim
|id=300644
|rsnum=104894845
|variant=0036
}}
{{omim
|id=300644
|rsnum=104894845
|variant=0057
}}{{ClinVar
|rsid=104894845
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=100656740
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=RPL36A-HNRNPH2:100529097; GLA:2717
|GENE_NAME=RPL36A-HNRNPH2; GLA
|GENE_ID=100529097; 2717
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.100656740C>G; NC_000023.10:g.100656740C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=874; 300644.0057; 2604; 300644.0036
|CLNSIG=5
|CLNCUI=C0002986
|CLNDBN=Fabry's disease; not provided
|Disease=Fabry's disease; not provided
|CLNACC=RCV000011516.1; RCV000078280.1; RCV000011495.1; RCV000078279.1
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1292:C0002986:301500:324:16652001
}}