{{Rsnum
|rsid=121908310
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GBA
|position=155205551
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=606463
|rsnum=121908310
|variant=0039
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000004544.1
|CLNALLE=1
|CLNDBN=Gaucher disease, perinatal lethal
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1269:C1842704:608013
|CLNHGVS=NC_000001.11:g.155235760C>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001005741.2:c.1309G>T; 606463.0039
|Disease=Gaucher disease
|FwdALT=T
|FwdREF=G
|GENEINFO=GBA:2629
|GENE_ID=2629
|GENE_NAME=GBA
|REF=C
|RSPOS=155235760
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05000002110100
|WGT=1
|dbSNPBuildID=133
|rsid=121908310
}}