ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 21 by Department of Human Genetics, Hannover Medical School

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_005422.4(TECTA):c.1779C>T (p.Ser593=)
NM_005422.4(TECTA):c.2101G>A (p.Gly701Ser)
NM_005422.4(TECTA):c.3338G>C (p.Gly1113Ala)
NM_005422.4(TECTA):c.36T>G (p.Ser12=) rs2135046516

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