{{Rsnum
|rsid = 28928872
|Gene = GGCX
|geno1 = (C;C)
|geno2 = (C;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|Chromosome=2
|position=85551919
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GGCX
}}{{omim
|desc=VITAMIN K-DEPENDENT COAGULATION DEFECT
|id=137167
|rsnum=28928872
|variant=0002
}}

{{ClinVar
|rsid=28928872
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=85779042
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=GGCX:2677
|GENE_NAME=GGCX
|GENE_ID=2677
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.85779042C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=137167.0002
|CLNSIG=5
|CLNCUI=C1848534
|CLNDBN=Vitamin k-dependent clotting factors, combined deficiency of, 1
|Disease=Vitamin k-dependent clotting factors
|CLNACC=RCV000017579.26
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1848534:277450:98434
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}