ClinVar Miner

List of variants in gene HNF4A reported as benign by Breakthrough Genomics, Breakthrough Genomics

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_175914.5(HNF4A):c.1217-67C>G rs3746575 0.56796
NM_175914.5(HNF4A):c.827-88T>C rs2273618 0.56736
NM_175914.5(HNF4A):c.1217-145T>C rs3746574 0.45705
NM_175914.5(HNF4A):c.50-38T>C rs736824 0.44632
NM_175914.5(HNF4A):c.*1132C>T rs6130615 0.24797
NM_175914.5(HNF4A):c.427-52G>A rs3212195 0.19516
NM_175914.5(HNF4A):c.320-204C>G rs13041396 0.19053
NM_175914.5(HNF4A):c.225-278A>G rs55934816 0.18308
NM_175914.5(HNF4A):c.427-96C>G rs3212194 0.15252
NM_175914.5(HNF4A):c.*392T>G rs11086926 0.13032
NM_175914.5(HNF4A):c.225-241C>T rs6093976 0.12430
NM_175914.5(HNF4A):c.*2366G>C rs3212211 0.11643
NM_175914.5(HNF4A):c.1217-151A>C rs74173201 0.07406
NM_175914.5(HNF4A):c.*242T>C rs41282030 0.04068
NM_175914.5(HNF4A):c.50-4538G>A rs113725562 0.03716
NM_175914.5(HNF4A):c.135C>T (p.Ala45=) rs736823 0.03705
NM_175914.5(HNF4A):c.50-4387A>C rs10427469 0.01810
NM_175914.5(HNF4A):c.319+19C>T rs112386711 0.01208
NM_175914.5(HNF4A):c.*155G>A rs41280258 0.01170
NM_175914.4(HNF4A):c.-276G>T rs148318607 0.00383
NM_175914.5(HNF4A):c.999C>T (p.Ile333=) rs150247632 0.00045
NM_175914.5(HNF4A):c.81C>T (p.Asn27=) rs570058788 0.00012
NM_175914.5(HNF4A):c.408G>A (p.Ala136=) rs374298096 0.00008
NM_175914.5(HNF4A):c.*906A>C rs3212210
NM_175914.5(HNF4A):c.*906A>T rs3212210

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