ClinVar Miner

Submissions for variant NM_001034853.2(RPGR):c.780G>T (p.Glu260Asp)

dbSNP: rs1328506002
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Erasmus University Medical Center RCV000984675 SCV000994768 uncertain significance Esophageal atresia; Pyloric stenosis 2019-05-22 no assertion criteria provided research

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