List of variants in gene HNF4A reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_175914.4(HNF4A):c.-401G>A	rs537336047	0.00320
NM_175914.5(HNF4A):c.726G>A (p.Val242=)	rs145280017	0.00041
NM_175914.5(HNF4A):c.-83C>T	rs879092890	0.00016
NM_175914.5(HNF4A):c.427-5C>T	rs374703326	0.00009
NM_175914.4(HNF4A):c.-378T>A	rs1048936817	0.00005
NM_175914.5(HNF4A):c.241G>A (p.Val81Met)	rs772786482	0.00005
NM_175914.5(HNF4A):c.445G>A (p.Gly149Arg)	rs747928745	0.00004
NM_175914.5(HNF4A):c.-18G>A	rs778173957	0.00003
NM_175914.5(HNF4A):c.1144G>A (p.Val382Ile)	rs377151067	0.00003
NM_175914.5(HNF4A):c.1267C>T (p.Pro423Ser)	rs1063239	0.00002
NM_175914.4(HNF4A):c.-426C>G	rs1193282686	0.00001
NM_175914.5(HNF4A):c.-44C>T	rs546252382	0.00001
NM_175914.5(HNF4A):c.-46C>A	rs764879208	0.00001
NM_175914.5(HNF4A):c.1177G>A (p.Gly393Arg)	rs757897768	0.00001
NM_175914.4(HNF4A):c.-171A>G	rs2146126988
NM_175914.4(HNF4A):c.-197G>A	rs2146126951
NM_175914.5(HNF4A):c.1081C>T (p.Pro361Ser)	rs761517690
NM_175914.5(HNF4A):c.1229C>A (p.Thr410Asn)	rs1313425622
NM_175914.5(HNF4A):c.1270T>C (p.Tyr424His)	rs1025249006
NM_175914.5(HNF4A):c.1303G>A (p.Val435Ile)	rs145314165
NM_175914.5(HNF4A):c.527T>C (p.Leu176Pro)
NM_175914.5(HNF4A):c.604G>A (p.Ala202Thr)
NM_175914.5(HNF4A):c.742G>T (p.Asp248Tyr)	rs2146445464
NM_175914.5(HNF4A):c.932G>T (p.Arg311Leu)

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