{{Rsnum
|rsid=121918333
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MED13L
|position=115969097
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MED13L
}}{{omim
|id=608771
|rsnum=121918333
|variant=0003
}}{{ClinVar
|rsid=121918333
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=116406902
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MED13L:23389
|GENE_NAME=MED13L
|GENE_ID=23389
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.116406902T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608771.0003
|CLNSIG=5
|CLNCUI=C1837341
|CLNDBN=Transposition of great arteries
|Disease=Transposition of great arteries
|CLNACC=RCV000002189.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1837341:608808
}}