{{Rsnum
|rsid=78973108
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GBA
|position=155207244
|Gene_s=GBA
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
}}{{ClinVar
|rsid=78973108
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=155237453
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000a05000402110100
|GENEINFO=GBA:2629
|GENE_NAME=GBA
|GENE_ID=2629
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155237453C>T
|CLNSRC=ClinVar; Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001005741.2:c.887G>A; 833; NBK1269; 606463.0041
|CLNSIG=5
|CLNCUI=C1842704; C1842704; C0017205; C0017205
|CLNDBN=Gaucher disease, perinatal lethal; Gaucher disease; not provided
|Disease=Gaucher disease; Gaucher disease; not provided
|CLNACC=RCV000004573.1; RCV000020159.1; RCV000079357.1
|Tags=PM;S3D;SLO;NSM;REF;ASP;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen
|CLNDSDBID=NBK1269:C1842704:608013; NBK1269:C0017205
}}