Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000371.4(TTR):c.424G>A (p.Val142Ile) | TTR | Pathogenic/Likely pathogenic | 18 | 29178618 | 29178618 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA214382,UniProtKB:P02766#VAR_007600,OMIM:176300.0009,ClinVar:1012273 |