List of variants in gene PAX8 reported as benign by GeneDx

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

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_003466.4(PAX8):c.390-103G>T	rs902691	0.99901
NM_003466.4(PAX8):c.1190-107A>C	rs4849175	0.99893
NM_003466.4(PAX8):c.191+94C>T	rs11678394	0.99683
NM_003466.4(PAX8):c.778-212T>C	rs11898670	0.97776
NM_003466.4(PAX8):c.1190-181G>A	rs4849176	0.40231
NM_003466.4(PAX8):c.25+24T>C	rs1867763	0.37329
NM_003466.4(PAX8):c.1088-337G>A	rs4849179	0.36946
NM_003466.4(PAX8):c.899-185T>G	rs7589901	0.34516
NM_003466.4(PAX8):c.1276+215C>T	rs2289897	0.22551
NM_003466.4(PAX8):c.898+195A>G	rs111501168	0.19123
NM_003466.4(PAX8):c.192-244A>G	rs67081417	0.17575
NM_003466.4(PAX8):c.1088-353G>C	rs4849180	0.17550
NM_003466.4(PAX8):c.898+99G>A	rs77270532	0.16900
NM_003466.4(PAX8):c.1189+138A>G	rs67776659	0.16577
NM_003466.4(PAX8):c.778-297G>A	rs13405033	0.15724
NM_003466.4(PAX8):c.778-163C>T	rs3738913	0.14518
NM_003466.4(PAX8):c.1189+229G>A	rs2241975	0.11067
NM_003466.4(PAX8):c.389+83T>C	rs13007173	0.07083
NM_003466.4(PAX8):c.*187A>G	rs78802229	0.05117
NM_003466.4(PAX8):c.478+135G>A	rs115905562	0.04886
NM_003466.4(PAX8):c.479-119T>C	rs118006067	0.04870
NM_003466.4(PAX8):c.479-68C>T	rs116441771	0.04804
NM_003466.4(PAX8):c.389+101G>A	rs74370449	0.04042
NM_003466.4(PAX8):c.1190-127G>A	rs76678068	0.01896
NM_003466.4(PAX8):c.1143C>T (p.Ser381=)	rs145036350	0.00516
NM_003466.4(PAX8):c.25+197G>T	rs2277884
NM_003466.4(PAX8):c.479-236_479-235del	rs3217557
NM_003466.4(PAX8):c.479-29C>A	rs13015478
NM_003466.4(PAX8):c.778-119C>A	rs1110839
NM_003466.4(PAX8):c.899-226G>C	rs7576384

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