List of variants in gene PAX9 reported as benign for tooth agenesis

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_006194.4(PAX9):c.-455C>G	rs4904155	0.37094
NM_001372076.1(PAX9):c.718G>C (p.Ala240Pro)	rs4904210	0.32799
NM_001372076.1(PAX9):c.*818C>T	rs11847165	0.18983
NM_001372076.1(PAX9):c.631+41G>A	rs2236007	0.16092
NC_000014.9:g.36659359C>A	rs34914085	0.15249
NM_001372076.1(PAX9):c.*554G>C	rs72679753	0.07300
NM_001372076.1(PAX9):c.*429T>C	rs17766200	0.07133
NM_001372076.1(PAX9):c.*259C>T	rs17104965	0.04118
NM_001372076.1(PAX9):c.*901C>T	rs17104971	0.03093
NM_001372076.1(PAX9):c.*206T>C	rs17104962	0.02868
NM_001372076.1(PAX9):c.516G>A (p.Lys172=)	rs61734510	0.00976
NM_001372076.1(PAX9):c.623C>G (p.Thr208Ser)	rs116676854	0.00784
NM_001372076.1(PAX9):c.609C>T (p.Gly203=)	rs61754301	0.00142
NM_001372076.1(PAX9):c.30G>A (p.Gln10=)	rs146561842	0.00045
NM_001372076.1(PAX9):c.717C>T (p.His239=)	rs12881240

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