{{Rsnum
|rsid=28362692
|Gene=AQP1
|Chromosome=7
|position=30912043
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.01561
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=AQP1
}}{{omim
|desc=COLTON BLOOD GROUP POLYMORPHISM
|id=107776
|rsnum=28362692
|variant=0001
}}

{{ClinVar
|rsid=28362692
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=30951658
|CHROM=7
|GMAF=0.0156
|dbSNPBuildID=125
|SSR=0
|SAO=1
|VP=0x050268000000140516110100
|GENEINFO=AQP1:358
|GENE_NAME=AQP1
|GENE_ID=358
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.30951658C>T
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;PMC;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9844; 0.01561
|CLNACC=RCV000019424.1
|CLNDBN=COLTON BLOOD GROUP POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=107776.0001
|COMMON=1
|Disease=COLTON BLOOD GROUP POLYMORPHISM
}}

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

{{GET Evidence
|gene=AQP1
|aa_change=Ala45Val
|aa_change_short=A45V
|impact=pharmacogenetic
|qualified_impact=Low clinical importance, Uncertain pharmacogenetic
|inheritance=other
|quality_scores=Array
|dbsnp_id=rs28362692
|overall_frequency_n=2
|overall_frequency_d=128
|overall_frequency=0.015625
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_vitro=2
|qualitycomment_in_vitro=Y
|qualityscore_case_control=0
|qualitycomment_case_control=Y
|qualityscore_severity=3
|qualitycomment_severity=Y
|qualityscore_treatability=4
|qualitycomment_treatability=Y
|in_omim=Y
|nblosum100=2
|autoscore=3
|webscore=N
|variant_evidence=0
|clinical_importance=0
|summary_short=Colton blood group polymorphism Co(b). This antigen system can sometimes be responsible for mild or moderate hemolytic transfusion reactions.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}