{{Rsnum
|rsid=62623459
|Gene=F2
|Chromosome=11
|position=46725897
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=F2
}}{{omim
|id=176930
|rsnum=62623459
|variant=0001
}}{{ClinVar
|rsid=62623459
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=46747447
|CHROM=11
|GMAF=0.0009
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=F2:2147
|GENE_NAME=F2
|GENE_ID=2147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.46747447G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNACC=RCV000014229.24
|CLNDBN=PROTHROMBIN TYPE 3
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176930.0001
|COMMON=0
|Disease=PROTHROMBIN TYPE 3
}}{{GET Evidence
|gene=F2
|aa_change=Glu200Lys
|aa_change_short=E200K
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs62623459
|overall_frequency_n=16
|overall_frequency_d=10758
|overall_frequency=0.00148726
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=3
|webscore=N
}}