List of variants reported as uncertain significance for Hypophosphatemic rickets, autosomal recessive, 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_004407.4(DMP1):c.815G>A (p.Arg272His)	rs145237146	0.00202
NM_004407.4(DMP1):c.1255C>T (p.Pro419Ser)	rs140275311	0.00036
NM_004407.4(DMP1):c.*159T>A	rs865870083	0.00030
NM_004407.4(DMP1):c.1502T>C (p.Ile501Thr)	rs146762807	0.00026
NM_004407.4(DMP1):c.428C>T (p.Thr143Ile)	rs370153862	0.00014
NM_004407.4(DMP1):c.517C>T (p.Arg173Trp)	rs200549155	0.00009
NM_004407.4(DMP1):c.1408G>A (p.Glu470Lys)	rs369921592	0.00001
NM_004407.4(DMP1):c.1490A>T (p.His497Leu)	rs376245118	0.00001
NM_004407.4(DMP1):c.709A>G (p.Met237Val)	rs201413886	0.00001
NM_004407.4(DMP1):c.1534G>A (p.Gly512Ser)	rs377414504
NM_004407.4(DMP1):c.1538A>G (p.Tyr513Cys)	rs1264750963

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