{{Rsnum
|rsid=6063
|Gene=FGG
|Chromosome=4
|position=154609725
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.006428
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FGG
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.9 | 99.1
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 1.8 | 98.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 4.0 | 96.0
| HapMapRevision=28
}}{{omim
|desc=FIBRINOGEN MILANO XII, DIGENIC
|id=134850
|rsnum=6063
|variant=0018
}}

This is the first snp to experiment with the watson alignment.

{{ watson alignment | preformatted=
<pre>r_gnl|ti|1767110221/265-275 AGAGCGGGCTT
gnl|ti|1846769777/267-277   AGAGCGGGCTT
gnl|ti|1832408368/258-268   NGAGCGGTCTT
gnl|ti|1797000559/116-126   AGAGCGGGCTT
gnl|dbSNP|rs6063/96-106     AGAGCRGGCTT
r_gnl|ti|1817651632/252-262 AAAAGGAAACT
                              *       *
</pre>
}}

{{ClinVar
|rsid=6063
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155530877
|CHROM=4
|GMAF=0.0064
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x050360000000050517110100
|GENEINFO=FGG:2266
|GENE_NAME=FGG
|GENE_ID=2266
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.155530877C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9936; 0.006428
|CLNACC=RCV000017800.1
|CLNDBN=Fibrinogen milano xii, digenic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134850.0018
|COMMON=1
|Disease=Fibrinogen milano xii
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}