ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.1192-1G>C

dbSNP: rs1601514990
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV001027996 SCV001190755 pathogenic Autosomal recessive nonsyndromic hearing loss 8 2020-02-05 no assertion criteria provided clinical testing

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