ClinVar Miner

Submissions for variant NM_001395656.1(ROBO2):c.928G>A (p.Val310Ile)

gnomAD frequency: 0.00003  dbSNP: rs780171319
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001461369 SCV001665269 likely benign not provided 2024-01-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005038229 SCV005660181 uncertain significance Vesicoureteral reflux 2 2024-03-27 criteria provided, single submitter clinical testing

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