{{Rsnum
|rsid=199474801
|Chromosome=11
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AGA)
|geno3=(AGA;AGA)
|Gene=TNNI2
|position=1841529
|Gene_s=TNNI2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199474801
|Reversed=0
|FwdREF=AGA
|FwdALT=
|REF=AAGA
|ALT=A
|RSPOS=1862755
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.1862759_1862761delAGA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191043.0004
|CLNSIG=5
|CLNCUI=C1834523
|CLNDBN=Distal arthrogryposis type 2B
|Disease=Distal arthrogryposis type 2B
|CLNACC=RCV000013251.15
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1834523:601680:1147
|GENEINFO=TNNI2:7136
|GENE_ID=7136
|GENE_NAME=TNNI2
}}{{PMID Auto
|PMID=16924011
|Title=A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis.
}}