{{Rsnum
|rsid=397515554
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MED12
|position=71127359
|Gene_s=MED12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000055909.1
|CLNALLE=1
|CLNDBN=FG syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1676:C0220769:305450:49984004
|CLNHGVS=NC_000023.10:g.70347209G>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1676
|Disease=FG syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=MED12:9968
|GENE_ID=9968
|GENE_NAME=MED12
|REF=G
|RSPOS=70347209
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515554
}}