ClinVar Miner

List of variants in gene ATP7B reported as likely pathogenic by Genetic Services Laboratory, University of Chicago

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000053.4(ATP7B):c.122A>G (p.Asn41Ser) rs201738967 0.00025
NM_000053.4(ATP7B):c.1877G>C (p.Gly626Ala) rs587783299 0.00006
NM_000053.4(ATP7B):c.4039G>A (p.Gly1347Ser) rs587783318 0.00004
NM_000053.4(ATP7B):c.3505A>G (p.Met1169Val) rs749085322 0.00002
NM_000053.4(ATP7B):c.1772G>A (p.Gly591Asp) rs797045402 0.00001
NM_000053.4(ATP7B):c.2002A>G (p.Met668Val) rs587783301

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