{{Rsnum
|rsid=78198234
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GBA
|position=155206211
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GBA
}}{{omim
|id=606463
|rsnum=78198234
|variant=0037
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000004569.1
|CLNALLE=1
|CLNDBN=Gaucher disease, perinatal lethal
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1269:C1842704:608013
|CLNHGVS=NC_000001.11:g.155236420T>C
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001005741.2:c.1049A>G; 606463.0037
|Disease=Gaucher disease
|FwdALT=G
|FwdREF=A
|GENEINFO=GBA:2629
|GENE_ID=2629
|GENE_NAME=GBA
|REF=T
|RSPOS=155236420
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;ASP;HD;OTHERKG;LSD;OM;NOC
|VC=SNV
|VP=0x050260000a05000402110110
|WGT=1
|dbSNPBuildID=131
|rsid=78198234
}}