{{Rsnum
|rsid=1799805
|Gene=ACHE
|Chromosome=7
|position=100893176
|Orientation=plus
|GMAF=0.02755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=ACHE
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 10.6 | 89.4
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 9.9 | 90.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 8.8 | 91.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 1.0 | 18.8 | 80.2
| HapMapRevision=28
}}{{omim
|id=100740
|rsnum=1799805
|variant=0001
}}

{{ClinVar
|rsid=1799805
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=100490797
|CHROM=7
|GMAF=0.0275
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x05036800000015051f110100
|GENEINFO=ACHE:43
|GENE_NAME=ACHE
|GENE_ID=43
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100490797G>T
|CLNORIGIN=1
|CLNSIG=2
|Tags=RV;PM;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9725; 0.02755
|CLNACC=RCV000020001.1
|CLNDBN=YT BLOOD GROUP POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=100740.0001
|COMMON=1
|Disease=YT BLOOD GROUP POLYMORPHISM
}}

{{PMID|21257350|OA=1
}} DNA-based methods in the immunohematology reference laboratory.

{{GET Evidence
|gene=ACHE
|aa_change=His353Asn
|aa_change_short=H353N
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1799805
|overall_frequency_n=368
|overall_frequency_d=10758
|overall_frequency=0.0342071
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=6
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=2
|n_web_uneval=10
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}