{{Rsnum
|rsid=74315310
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FCGR1A
|position=149784224
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FCGR1A,HIST2H2BF
}}{{omim
|id=146760
|rsnum=74315310
|variant=0001
}}{{ClinVar
|rsid=74315310
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=149784224
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260080605040002110100
|GENEINFO=HIST2H2BF:440689; FCGR1A:2209
|GENE_NAME=HIST2H2BF; FCGR1A
|GENE_ID=440689; 2209
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.149784224C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;NSN;REF;INT;ASP;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000015950.24; RCV000015951.24
|CLNDBN=Igg receptor i, phagocytic, familial deficiency of; Cd64 deficiency, familial
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000566.3:c.274C>T; 146760.0001
|Disease=Igg receptor i; Cd64 deficiency
}}