List of variants reported as likely pathogenic for ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001282531.3(ADNP):c.1310dup (p.Gly438fs)	rs2122753883
NM_001282531.3(ADNP):c.2089dup (p.Gln697fs)	rs2122747616
NM_001282531.3(ADNP):c.2938C>T (p.Gln980Ter)	rs1980763449
NM_001282531.3(ADNP):c.64dup (p.Ile22fs)	rs1982229334
NM_001282531.3(ADNP):c.709del (p.Val237fs)	rs1981116316

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