List of variants in gene HNF4A reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_175914.5(HNF4A):c.84G>A (p.Ala28=)	rs41282026	0.00084
NM_175914.5(HNF4A):c.999C>T (p.Ile333=)	rs150247632	0.00045
NM_175914.5(HNF4A):c.138G>A (p.Thr46=)	rs145845882	0.00043
NM_175914.5(HNF4A):c.921C>T (p.Asp307=)	rs151168174	0.00039
NM_175914.5(HNF4A):c.1176C>T (p.Asn392=)	rs141448616	0.00033
NM_175914.5(HNF4A):c.50-4753G>A	rs566155738	0.00016
NM_175914.5(HNF4A):c.670+7C>T	rs376544046	0.00005
NM_175914.5(HNF4A):c.50-4665C>T	rs774093087	0.00003
NM_175914.5(HNF4A):c.138G>T (p.Thr46=)
NM_175914.5(HNF4A):c.50-3406A>G
NM_175914.5(HNF4A):c.50-4562G>A
NM_175914.5(HNF4A):c.50-4563G>A
NM_175914.5(HNF4A):c.50-4746G>A
NM_175914.5(HNF4A):c.50-4747C>G
NM_175914.5(HNF4A):c.50-4754C>G
NM_175914.5(HNF4A):c.50-4758A>G
NM_175914.5(HNF4A):c.50-4G>A
NM_175914.5(HNF4A):c.670+18C>A	rs751211080
NM_175914.5(HNF4A):c.827-6T>C
NM_175914.5(HNF4A):c.952C>T (p.Leu318=)

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