{{Rsnum
|rsid=79653797
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GBA
|position=155208420
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GBA
}}{{omim
|id=606463
|rsnum=79653797
|variant=0004
}}{{ClinVar
|rsid=79653797
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155238629
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000a05000402110110
|GENEINFO=GBA:2629
|GENE_NAME=GBA
|GENE_ID=2629
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155238629C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001005741.2:c.476G>A; NBK1269; 606463.0004
|CLNSIG=5
|CLNCUI=C1961835; C1961835; C1842704; C1842704
|CLNDBN=Gaucher's disease, type 1; Gaucher disease, perinatal lethal; Gaucher disease
|Disease=Gaucher's disease; Gaucher disease; Gaucher disease
|CLNACC=RCV000004518.3; RCV000004519.3; RCV000020154.1
|Tags=RV;PM;S3D;SLO;NSM;REF;ASP;HD;OTHERKG;LSD;OM;NOC
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM; GeneReviews:MedGen
|CLNDSDBID=NBK1269:C1961835:230800:ORPHA355:ORPHA77259:62201009; NBK1269:C1842704:608013; NBK1269:C0017205
}}