{{Rsnum
|rsid=121434634
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PLA2G4A
|position=186894164
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PLA2G4A
}}{{omim
|id=600522
|rsnum=121434634
|variant=0001
}}{{ClinVar
|rsid=121434634
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=186894164
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=PLA2G4A:5321
|GENE_NAME=PLA2G4A
|GENE_ID=5321
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.186894164T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000009647.1
|CLNDBN=PHOSPHOLIPASE A2, GROUP IV A, DEFICIENCY OF
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_024420.2:c.331T>C; 600522.0001
|Disease=PHOSPHOLIPASE A2
}}