Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000545.8(HNF1A):c.365A>G (p.Tyr122Cys) | HNF1A | Likely pathogenic | 12 | 121426674 | 121426674 | A | G | reviewed by expert panel | ClinGen:CA124457,OMIM:142410.0004 |