List of variants in gene PHEX reported as benign for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
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.10G>C (p.Glu4Gln)	rs147859619	0.00030
NM_000444.6(PHEX):c.631G>A (p.Asp211Asn)	rs370610267	0.00019
NM_000444.6(PHEX):c.957G>A (p.Lys319=)	rs373261521	0.00012
NM_000444.6(PHEX):c.118+7G>T	rs534550003	0.00006
NM_000444.6(PHEX):c.1174-10_1174-1del
NM_000444.6(PHEX):c.1241del (p.Leu414fs)	rs886041446
NM_000444.6(PHEX):c.1318G>T (p.Glu440Ter)
NM_000444.6(PHEX):c.1536T>G (p.Tyr512Ter)
NM_000444.6(PHEX):c.1645C>T (p.Arg549Ter)	rs886041224
NM_000444.6(PHEX):c.188-2A>C
NM_000444.6(PHEX):c.208_212del (p.Val70fs)	rs1927568587
NM_000444.6(PHEX):c.292dup (p.Met98fs)
NM_000444.6(PHEX):c.436+4A>G	rs1057520344
NM_000444.6(PHEX):c.846del (p.Glu283fs)
NM_000444.6(PHEX):c.871C>T (p.Arg291Ter)	rs866429868

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