List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 1 by New York Genome Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378120.1(MBD5):c.826C>T (p.Pro276Ser)	rs376756158	0.00014
NM_001378120.1(MBD5):c.763C>T (p.Pro255Ser)	rs183855575	0.00012
GRCh38/hg38 2q23.1(chr2:148120444-148180182)
NM_001378120.1(MBD5):c.136T>C (p.Cys46Arg)	rs139186486
NM_001378120.1(MBD5):c.2237C>G (p.Ser746Cys)	rs2105641052

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