ClinVar Miner

List of variants studied for Hearing loss, autosomal recessive 113

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001039213.4(CEACAM16):c.703C>T (p.Arg235Cys) rs746164064 0.00004
NM_001039213.4(CEACAM16):c.1057G>A (p.Gly353Arg) rs777655944 0.00002
NM_001039213.4(CEACAM16):c.37G>T (p.Ala13Ser) rs1198256157
NM_001039213.4(CEACAM16):c.662-1G>C rs1568528171

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