List of variants in gene PDHX reported as likely benign by GeneDx

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_003477.3(PDHX):c.1183-297A>G	rs114785241	0.01115
NM_003477.3(PDHX):c.1247+210G>A	rs79133843	0.00817
NM_003477.3(PDHX):c.241+59_241+60insG	rs199912895	0.00805
NM_003477.3(PDHX):c.542+97A>G	rs11032951	0.00666
NM_003477.3(PDHX):c.241+173G>A	rs77452052	0.00451
NM_003477.3(PDHX):c.817-43A>G	rs114136993	0.00364
NM_003477.3(PDHX):c.1248-76A>G	rs60250721	0.00321
NM_003477.3(PDHX):c.*27A>C	rs74524673	0.00299
NM_003477.3(PDHX):c.1024-38C>T	rs111818080	0.00277
NM_003477.3(PDHX):c.641+33A>G	rs190828200	0.00270
NM_003477.3(PDHX):c.474G>A (p.Glu158=)	rs148723565	0.00243
NM_003477.3(PDHX):c.343-49G>A	rs200728017	0.00235
NM_003477.3(PDHX):c.642-19A>G	rs138324257	0.00151
NM_003477.3(PDHX):c.618C>G (p.Gly206=)	rs143997835	0.00126
NM_003477.3(PDHX):c.161-6T>C	rs200438675	0.00056
NM_003477.3(PDHX):c.749C>T (p.Thr250Ile)	rs146876119	0.00039
NM_003477.3(PDHX):c.640G>C (p.Glu214Gln)	rs146445744	0.00036
NM_003477.3(PDHX):c.411T>C (p.Asp137=)	rs145394719	0.00021
NM_003477.3(PDHX):c.542+10T>C	rs368960575	0.00021
NM_003477.3(PDHX):c.532G>A (p.Gly178Arg)	rs765182974	0.00011
NM_003477.3(PDHX):c.526A>G (p.Ile176Val)	rs767427196	0.00004
NM_003477.3(PDHX):c.1248-15T>C	rs749908412	0.00002
NM_003477.3(PDHX):c.789A>G (p.Val263=)	rs755428861	0.00002
NM_003477.3(PDHX):c.1266G>A (p.Met422Ile)	rs533512853	0.00001
NM_003477.3(PDHX):c.241+15T>A	rs543696996	0.00001
NM_003477.3(PDHX):c.675G>A (p.Thr225=)	rs558284287	0.00001
NM_003477.3(PDHX):c.161-10dup	rs771708416
NM_003477.3(PDHX):c.161-280dup	rs200608148
NM_003477.3(PDHX):c.241+55_241+56dup	rs368865759
NM_003477.3(PDHX):c.462A>G (p.Ser154=)	rs1554987626
NM_003477.3(PDHX):c.642-283_642-281dup	rs539430741
NM_003477.3(PDHX):c.769C>A (p.Arg257=)	rs768910663
NM_003477.3(PDHX):c.828T>G (p.Thr276=)	rs1554989176

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