{{Rsnum
|rsid=368060
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=GBA
|position=155205008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GBA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 0.0 | 4.8 | 95.2
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 1.7 | 98.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=606463
|rsnum=368060
|variant=0009
}}{{ClinVar
|rsid=368060
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=155235217
|CHROM=1
|dbSNPBuildID=80
|SSR=0
|SAO=1
|VP=0x050360000000040103110100
|GENEINFO=GBA:2629
|GENE_NAME=GBA
|GENE_ID=2629
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155235217C>G
|CLNSRC=ClinVar; Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001005741.2:c.1483G>C; 791; 606463.0009
|CLNSIG=5
|CLNCUI=C1961835; C1961835; C1961835; C0268250; C0268250; C0268250; C0268251; C0268251; C0268251; C1842704; C1842704; C1842704
|CLNDBN=Gaucher's disease, type 1; Acute neuronopathic Gaucher's disease; Subacute neuronopathic Gaucher's disease; Gaucher disease, perinatal lethal; AllHighlyPenetrant
|Disease=Gaucher's disease; Acute neuronopathic Gaucher's disease; Subacute neuronopathic Gaucher's disease; Gaucher disease; AllHighlyPenetrant
|CLNACC=RCV000004533.3; RCV000004534.3; RCV000004535.3; RCV000004536.3; RCV000079341.1
|Tags=PM;S3D;SLO;VLD;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1269:C1961835:230800:ORPHA355:ORPHA77259:62201009; NBK1269:C0268250:230900:12246008; NBK1269:C0268251:231000:ORPHA355:ORPHA77261:5963005; NBK1269:C1842704:608013
}}