{{Rsnum
|rsid=121434635
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PLA2G4A
|position=186956219
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PLA2G4A
}}{{omim
|id=600522
|rsnum=121434635
|variant=0002
}}{{ClinVar
|rsid=121434635
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=186956219
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260080a05000002110100
|GENEINFO=PLA2G4A:5321
|GENE_NAME=PLA2G4A
|GENE_ID=5321
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.186956219G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000009648.1
|CLNDBN=PHOSPHOLIPASE A2, GROUP IV A, DEFICIENCY OF
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_024420.2:c.1454G>A; 600522.0002
|Disease=PHOSPHOLIPASE A2
}}