{{Rsnum
|rsid=28374544
|Gene=ZFPM2
|Chromosome=8
|position=105802051
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.03306
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZFPM2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 70.5 | 26.0 | 3.4
| ASW | 75.4 | 24.6 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 70.6 | 27.5 | 1.8
| MEX | 0.0 | 0.0 | 0.0
| MKK | 86.5 | 12.8 | 0.6
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=TETRALOGY OF FALLOT
|id=603693
|rsnum=28374544
|variant=0001
}}

{{ClinVar
|rsid=28374544
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=106814279
|CHROM=8
|GMAF=0.0334
|dbSNPBuildID=125
|SSR=0
|SAO=1
|VP=0x05016000000017051f110100
|GENEINFO=ZFPM2:23414
|GENE_NAME=ZFPM2
|GENE_ID=23414
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.106814279A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603693.0001
|CLNSIG=5
|CLNCUI=C0039685
|CLNDBN=Tetralogy of Fallot
|Disease=Tetralogy of Fallot
|CLNACC=RCV000006501.1
|Tags=PM;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9669; 0.03306
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0039685:187500:3303:86299006
|COMMON=1
}}

{{GET Evidence
|gene=ZFPM2
|aa_change=Ser657Gly
|aa_change_short=S657G
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=other
|quality_scores=Array
|dbsnp_id=rs28374544
|overall_frequency_n=407
|overall_frequency_d=9644
|overall_frequency=0.0422024
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=1
|qualitycomment_in_silico=Y
|qualityscore_in_vitro=1
|qualitycomment_in_vitro=Y
|qualityscore_case_control=0
|qualitycomment_case_control=Y
|qualityscore_severity=5
|qualitycomment_severity=Y
|qualityscore_treatability=4
|qualitycomment_treatability=Y
|in_omim=Y
|nblosum100=2
|autoscore=3
|webscore=N
|summary_short=This variant is associated with Tetralogy of Fallot which typically has low penetrance alleles. High frequency in HapMap and 1000 genomes (11.4% and 18.8%, respectively) seems to contradict pathogenic hypothesis.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}