{{Rsnum
|rsid=79977247
|Chromosome=18
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TTR
|position=31592975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TTR
}}{{omim
|id=176300
|rsnum=79977247
|variant=0014
}}
{{omim
|id=176300
|rsnum=79977247
|variant=0049
}}{{ClinVar
|rsid=79977247
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=29172938
|CHROM=18
|dbSNPBuildID=131
|SSR=16
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=TTR:7276
|GENE_NAME=TTR
|GENE_ID=7276
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000018.9:g.29172938T>C; NC_000018.9:g.29172938T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176300.0014; 176300.0049
|CLNSIG=5
|CLNCUI=C2751492
|CLNDBN=Amyloidogenic transthyretin amyloidosis; AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
|Disease=Amyloidogenic transthyretin amyloidosis; AMYLOIDOSIS
|CLNACC=RCV000014372.24; RCV000014407.22
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1194:C2751492:105210:85447:85451:16573007:43532007:442012008
}}