{{Rsnum
|rsid=121909675
|Chromosome=2
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GGCX
|position=85553045
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GGCX
}}{{omim
|id=137167
|rsnum=121909675
|variant=0001
}}{{ClinVar
|rsid=121909675
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=85780168
|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.85780168A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=137167.0001
|CLNSIG=5
|CLNCUI=C1848534
|CLNDBN=Vitamin k-dependent clotting factors, combined deficiency of, 1
|Disease=Vitamin k-dependent clotting factors
|CLNACC=RCV000017578.26
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1848534:277450:98434
}}