ClinVar Miner

List of variants reported as likely pathogenic for Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant; Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive by Invitae

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NC_000001.10:g.(?_236631511)_(236631596_?)dup
NM_145861.4(EDARADD):c.367G>A (p.Asp123Asn) rs879255629

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