ClinVar Miner

Submissions for variant NM_004839.4(HOMER2):c.799_803del (p.Pro267fs)

dbSNP: rs2051382999
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics Department, Hospital Ramon y Cajal-IRYCIS RCV001327994 SCV001499845 pathogenic Autosomal dominant nonsyndromic hearing loss 68 2021-03-07 no assertion criteria provided clinical testing

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