Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000210738 | SCV000263034 | likely pathogenic | Inborn genetic diseases | criteria provided, single submitter | clinical testing | LIKELY POSITIVE: Relevant Alteration(s) Detected | |
OMIM | RCV000761193 | SCV000891109 | risk factor | Epilepsy, idiopathic generalized, susceptibility to, 15 | 2019-03-14 | no assertion criteria provided | literature only |