Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NC_000010.11:g.(?_43100449)_(43102639_?)del | RET | Likely pathogenic | 10 | 43595897 | 43598087 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_020975.6(RET):c.1879+1G>A | RET | Pathogenic/Likely pathogenic | 10 | 43609124 | 43609124 | G | A | criteria provided, multiple submitters, no conflicts | - |