{{Rsnum
|rsid=364897
|Gene=GBA
|Chromosome=1
|position=155208006
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GBA
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 13.0 | 59.3 | 27.8
| HCB | 4.7 | 30.2 | 65.1
| JPT | 0.0 | 32.5 | 67.5
| YRI | 15.8 | 57.9 | 26.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.7 | 30.2 | 65.1
| 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
}}

[[rs364897]], also known as Asn188Ser or N188S, is a variant in the [[GBA]] gene. [[rs354897]](A) encodes the more common Asn at this position.

[[rs364897]](G;G) has been observed in Korean and Taiwanese subjects with type I [[Gaucher disease]].{{PMID|8829654}}

It may be a relatively mild defect in the gene, since it appears the encoded enzyme appears to retain most of its function.{{PMID|15146461}}

{{omim
|id=606463
|rsnum=364897
|variant=0026
}}

{{ClinVar
|rsid=364897
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=155238215
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=80
|SSR=0
|SAO=1
|VP=0x050368000a05050517110110
|GENEINFO=GBA:2629
|GENE_NAME=GBA
|GENE_ID=2629
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.155238215T>C
|CLNSRC=ClinVar; Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001005741.2:c.680A>G; 797; NBK1269; 606463.0026
|CLNSIG=5
|CLNCUI=C1961835; C1961835; C0268251; C0268251; C0017205; C0017205
|CLNDBN=Gaucher's disease, type 1; Subacute neuronopathic Gaucher's disease; Gaucher disease; not provided
|Disease=Gaucher's disease; Subacute neuronopathic Gaucher's disease; Gaucher disease; not provided
|CLNACC=RCV000004557.3; RCV000004558.3; RCV000020156.1; RCV000079352.1
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM;NOC
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK1269:C1961835:230800:ORPHA355:ORPHA77259:62201009; NBK1269:C0268251:231000:ORPHA355:ORPHA77261:5963005; NBK1269:C0017205
|COMMON=0
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}