List of variants in gene DMP1 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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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.639G>A (p.Glu213=)	rs116732769	0.00193
NM_004407.4(DMP1):c.600G>A (p.Gly200=)	rs34682707	0.00111
NM_004407.4(DMP1):c.1255C>T (p.Pro419Ser)	rs140275311	0.00036
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.135+1G>T	rs141480996	0.00013
NM_004407.4(DMP1):c.*159T>A	rs865870083	0.00010
NM_004407.4(DMP1):c.517C>T (p.Arg173Trp)	rs200549155	0.00009
NM_004407.4(DMP1):c.55-1G>C	rs587776697	0.00002
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
NM_004407.4(DMP1):c.844C>A (p.Leu282Ile)	rs141979823

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