{{Rsnum
|rsid=1064644
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GBA
|position=155207983
|Gene_s=GBA
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| 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
}}{{ClinVar
|rsid=1064644
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=155238192
|CHROM=1
|dbSNPBuildID=86
|SSR=1
|SAO=1
|VP=0x050368000a05000103110140
|GENEINFO=GBA:2629
|GENE_NAME=GBA
|GENE_ID=2629
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155238192A>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=608013
|CLNDBN=Gaucher disease
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;GNO;OTHERKG;PH3;LSD;OM
|CLNACC=RCV000020157.1
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1269:C0017205
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_001005741.2:c.703T>C; NBK1269
|Disease=Gaucher disease
}}

{{PMID Auto
|PMID=10685993
|Title=Type 2 Gaucher disease: the collodion baby phenotype revisited.
|OA=1
}}

{{omim
|id=608013
|rsnum=1064644
}}

{{on chip | 23andMe v3}}