ClinVar Miner

Submissions for variant NM_024915.4(GRHL2):c.34G>T (p.Val12Leu)

dbSNP: rs749906501
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Otology & Neurotology- Genomics of vestibular disorders (CTS-495), Jose Antonio López Escámez, Centro Pfizer - Universidad de Granada - Junta de Andalucía de Genómica e Investigación Oncológica (GENYO) RCV000416587 SCV000323083 uncertain significance Progressive sensorineural hearing impairment 2016-09-03 no assertion criteria provided research

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