List of variants in gene PHEX reported as 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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000444.6(PHEX):c.-90A>G	rs178710	0.51407
NM_000444.6(PHEX):c.1302+277G>A	rs6528091	0.40285
NM_000444.6(PHEX):c.1586+287G>T	rs7881294	0.24625
NM_000444.6(PHEX):c.1080-73C>T	rs4824224	0.22096
NM_000444.6(PHEX):c.1482+271G>A	rs73636814	0.20941
NM_000444.6(PHEX):c.188-291T>G	rs178719	0.19177
NM_000444.6(PHEX):c.118+317T>C	rs5951685	0.17749
NM_000444.6(PHEX):c.1174-286G>A	rs10218272	0.17340
NM_000444.6(PHEX):c.188-47C>T	rs178720	0.17091
NM_000444.6(PHEX):c.1174-218T>G	rs10217954	0.15562
NM_000444.6(PHEX):c.-33C>T	rs5951494	0.13118
NM_000444.6(PHEX):c.1645+174T>G	rs2071583	0.11891
NM_000444.6(PHEX):c.1079+213T>C	rs45541842	0.10369
NM_000444.6(PHEX):c.733-189G>A	rs6528089	0.09431
NM_000444.6(PHEX):c.933+41A>G	rs58524357	0.09168
NM_000444.6(PHEX):c.933+286G>A	rs73636804	0.08955
NM_000444.6(PHEX):c.664-124G>C	rs12013780	0.08886
NM_000444.6(PHEX):c.849+128G>A	rs6629449	0.08782
NM_000444.6(PHEX):c.934-217A>C	rs7052268	0.07744
NM_000444.6(PHEX):c.849+1049T>C	rs73635602	0.07640
NM_000444.6(PHEX):c.437-208A>G	rs57027136	0.07450
NM_000444.6(PHEX):c.1079+279C>T	rs7882590	0.06506
NM_000444.6(PHEX):c.1645+110G>T	rs16981826	0.05979
NM_000444.6(PHEX):c.1483-211G>T	rs41311821	0.04153
NM_000444.6(PHEX):c.1645+169C>T	rs113381174	0.02602
NM_000444.6(PHEX):c.1174-307T>C	rs143973252	0.01964
NM_000444.6(PHEX):c.1206A>G (p.Gln402=)	rs151234075	0.00986
NM_000444.6(PHEX):c.288A>G (p.Glu96=)	rs112836831	0.00980
NM_000444.6(PHEX):c.489A>G (p.Ser163=)	rs140231382	0.00748
NM_000444.6(PHEX):c.537T>A (p.Val179=)	rs137961493	0.00746
NM_000444.6(PHEX):c.1515C>T (p.Asn505=)	rs764771688	0.00001
NM_000444.6(PHEX):c.118+286del	rs3216804
NM_000444.6(PHEX):c.1483-312=	rs5951715
NM_000444.6(PHEX):c.1645+212A>G	rs16981831
NM_000444.6(PHEX):c.399G>A (p.Gln133=)	rs1602273860

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