List of variants in gene DMP1 reported as benign for Hypophosphatemic rickets, autosomal recessive, 1

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_004407.4(DMP1):c.*607A>G	rs2627725	0.61047
NM_004407.4(DMP1):c.205A>T (p.Ser69Cys)	rs10019009	0.29735
NM_004407.4(DMP1):c.1230G>A (p.Glu410=)	rs2615497	0.28028
NM_004407.4(DMP1):c.*35G>A	rs2627724	0.27831
NM_004407.4(DMP1):c.1218C>T (p.Ser406=)	rs2615498	0.15334
NM_004407.4(DMP1):c.*905A>G	rs73843105	0.04782
NM_004407.4(DMP1):c.*280C>T	rs76370957	0.04084
NM_004407.4(DMP1):c.*457T>C	rs6842411	0.02615
NM_004407.4(DMP1):c.*329A>C	rs6816379	0.02610
NM_004407.4(DMP1):c.*603C>T	rs78837592	0.01450
NM_004407.4(DMP1):c.1388A>G (p.Lys463Arg)	rs34661425	0.01341
NM_004407.4(DMP1):c.475C>A (p.Gln159Lys)	rs79402270	0.00466
NM_004407.4(DMP1):c.*380C>T	rs150349595	0.00387
NM_004407.4(DMP1):c.600G>A (p.Gly200=)	rs34682707	0.00111
NM_004407.4(DMP1):c.1448A>C (p.Asn483Thr)	rs574215585	0.00001
NM_004407.4(DMP1):c.844C>A (p.Leu282Ile)	rs141979823

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