List of variants in gene PAX4 reported as benign for monogenic diabetes

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001366110.1(PAX4):c.*521C>T	rs712699	0.74699
NM_001366110.1(PAX4):c.986A>C (p.His329Pro)	rs712701	0.74316
NM_001366110.1(PAX4):c.*211A>G	rs712700	0.74220
NM_001366110.1(PAX4):c.*477C>T	rs327520	0.29767
NM_001366110.1(PAX4):c.421C>T (p.Arg141Trp)	rs2233578	0.02460
NM_001366110.1(PAX4):c.599G>A (p.Arg200His)	rs2233580	0.00220
NM_001366110.1(PAX4):c.385C>T (p.Arg129Trp)	rs114202595	0.00013
NM_001366110.1(PAX4):c.*469TATG[3]	rs66998513
NM_001366110.1(PAX4):c.477_478insATGT	rs200757052
NM_001366110.1(PAX4):c.13+175G>C	rs327516
NM_001366110.1(PAX4):c.598C>A (p.Arg200Ser)	rs3824004
NM_001366110.1(PAX4):c.772-13dup	rs35434068

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