{{Rsnum
|rsid=76863441
|Gene=PLA2G7
|Chromosome=6
|position=46709361
|Orientation=plus
|GMAF=0.02984
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=PLA2G7
}}{{omim
|id=601690
|rsnum=76863441
|variant=0001
}}{{ClinVar
|rsid=76863441
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=46677098
|CHROM=6
|GMAF=0.0298
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000150516110100
|GENEINFO=PLA2G7:7941
|GENE_NAME=PLA2G7
|GENE_ID=7941
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.46677098C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601690.0001
|CLNSIG=5
|CLNCUI=C1866472
|CLNDBN=Platelet-activating factor acetylhydrolase deficiency
|Disease=Platelet-activating factor acetylhydrolase deficiency
|CLNACC=RCV000008376.1
|Tags=PM;PMC;S3D;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9702; 0.02984
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1866472:614278
|COMMON=1
}}
{{ population diversity
| geno1 = (A;A)
| geno2 = (A;C)
| geno3 = (C;C)
| CEU | 0.0 | 1.7 | 98.3
| HCB | 0.0 | 4.4 | 95.6
| JPT | 2.2 | 31.1 | 66.7
| YRI | 0.0 | 3.3 | 96.7
| ASW | 0 | 0 | 0
| CHD | 0 | 0 | 0
| GIH | 0 | 0 | 0
| LWK | 0 | 0 | 0
| MEX | 0 | 0 | 0
| MKK | 0 | 0 | 0
| TSI | 0 | 0 | 0
}}{{PMID Auto
|PMID=23404648
|Title=An association study between genetic polymorphisms related to lipoprotein-associated phospholipase A(2) and coronary heart disease.
|OA=1
}}