List of variants in gene PAX4 reported as uncertain significance for Maturity onset diabetes mellitus in young

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001366110.1(PAX4):c.986A>C (p.His329Pro)	rs712701	0.74681
NM_001366110.1(PAX4):c.474C>T (p.Gly158=)	rs77039439	0.04703
NM_001366110.1(PAX4):c.313C>T (p.Arg105Cys)	rs144792551	0.00074
NM_001366110.1(PAX4):c.14-182G>A	rs886061971	0.00025
NM_001366110.1(PAX4):c.260G>A (p.Arg87Gln)	rs115923648	0.00022
NM_001366110.1(PAX4):c.1014C>T (p.Ala338=)	rs201607054	0.00013
NM_001366110.1(PAX4):c.1024C>T (p.Pro342Ser)	rs143084654	0.00010
NM_001366110.1(PAX4):c.14-51G>A	rs878919319	0.00008
NM_001366110.1(PAX4):c.572G>A (p.Arg191His)	rs145284016	0.00006
NM_001366110.1(PAX4):c.14-101C>T	rs886061970	0.00003
NM_001366110.1(PAX4):c.14-176C>A	rs754931916	0.00003
NM_001366110.1(PAX4):c.515G>A (p.Arg172Gln)	rs587780414	0.00001
NM_001366110.1(PAX4):c.474_477dup	rs1554403669
NM_001366110.1(PAX4):c.492_497del	rs886061966
NM_001366110.1(PAX4):c.*494AC[11]	rs36159526
NM_001366110.1(PAX4):c.*494AC[13]	rs36159526
NM_001366110.1(PAX4):c.*494AC[14]	rs36159526
NM_001366110.1(PAX4):c.514_521delinsTGAT	rs886061965
NM_001366110.1(PAX4):c.518_521delinsACACTGAT	rs886061964
NM_001366110.1(PAX4):c.*66C>T	rs886061967
NM_001366110.1(PAX4):c.*722T>C	rs759186282
NM_001366110.1(PAX4):c.403C>G (p.Gln135Glu)	rs886061969
NM_001366110.1(PAX4):c.772-13dup	rs35434068
NM_001366110.1(PAX4):c.772-3del	rs35434068
NM_001366110.1(PAX4):c.904C>A (p.Pro302Thr)	rs886061968

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