ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.1149+1G>A

dbSNP: rs2535317969
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003472912 SCV004204240 pathogenic Autosomal recessive nonsyndromic hearing loss 4 2022-12-13 criteria provided, single submitter clinical testing
Precision Medicine Center, Zhengzhou University RCV003472912 SCV005049548 likely pathogenic Autosomal recessive nonsyndromic hearing loss 4 2024-06-01 criteria provided, single submitter clinical testing

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