ClinVar Miner

List of variants in gene DMP1 reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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