List of variants in gene SLC34A3 reported as benign for hereditary hypophosphatemic rickets with hypercalciuria

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001177316.2(SLC34A3):c.1538A>T (p.Glu513Val)	rs28542318	0.88574
NM_001177316.2(SLC34A3):c.757T>C (p.Leu253=)	rs28407527	0.42407
NM_001177316.2(SLC34A3):c.625C>T (p.Leu209=)	rs34796681	0.00467
NM_001177316.2(SLC34A3):c.1585A>T (p.Ile529Phe)	rs140639805	0.00216
NM_001177316.2(SLC34A3):c.1454G>A (p.Arg485His)	rs138872455	0.00215
NM_001177316.2(SLC34A3):c.1210+17G>A	rs202071967
NM_001177316.2(SLC34A3):c.942G>C (p.Ala314=)	rs34664302

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