{{Rsnum
|rsid=28935490
|Gene=GLA
|Chromosome=X
|position=101398432
|Orientation=plus
|GMAF=0.001209
|Gene_s=GLA,RPL36A-HNRNPH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{omim
|id=300644
|rsnum=28935490
|variant=0026
}}

{{ClinVar
|rsid=28935490
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=100653420
|CHROM=X
|GMAF=0.00120555
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000040016110100
|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.100653420C>A
|CLNORIGIN=1
|Tags=RV;PM;PMC;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9988; 0.001209
|CLNACC=RCV000011486.2; RCV000029944.1; RCV000035314.1
|CLNDBN=Reclassified - variant of unknown significance; Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
|CLNSIG=4
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300644.0026
|COMMON=0
|Disease=Reclassified - variant of unknown significance; Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
}}

{{PMID|18154965}} Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy.

{{PMID|19377476|OA=1
}} A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}