List of variants reported as likely benign for Hypodontia

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001372076.1(PAX9):c.428A>G (p.Tyr143Cys)	rs139008563	0.00023
NM_001372076.1(PAX9):c.192C>T (p.Gly64=)	rs200688741	0.00019
NM_001372076.1(PAX9):c.511G>A (p.Ala171Thr)	rs143020311	0.00010
NM_001372076.1(PAX9):c.774A>T (p.Ala258=)	rs750664427	0.00007
NM_001372076.1(PAX9):c.679A>C (p.Ser227Arg)	rs199777734	0.00006
NM_001372076.1(PAX9):c.640A>G (p.Ser214Gly)	rs375436662	0.00001
NM_001372076.1(PAX9):c.123C>T (p.Asp41=)
NM_001372076.1(PAX9):c.156C>T (p.Cys52=)
NM_001372076.1(PAX9):c.393C>T (p.Ile131=)
NM_001372076.1(PAX9):c.438C>T (p.His146=)
NM_001372076.1(PAX9):c.45C>T (p.Phe15=)
NM_001372076.1(PAX9):c.480C>T (p.Tyr160=)
NM_001372076.1(PAX9):c.606G>A (p.Leu202=)
NM_001372076.1(PAX9):c.684G>A (p.Leu228=)
NM_001372076.1(PAX9):c.771+20G>T
NM_001372076.1(PAX9):c.954G>A (p.Pro318=)

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