Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000210680 | SCV000263033 | pathogenic | Inborn genetic diseases | 2016-07-20 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000761192 | SCV000891108 | risk factor | Epilepsy, idiopathic generalized, susceptibility to, 15 | 2019-03-14 | no assertion criteria provided | literature only |