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.229G>A (p.Gly77Arg) | TTR | Pathogenic | 18 | 29175111 | 29175111 | G | A | criteria provided, single submitter | - |