ClinVar Miner

List of variants reported as benign for arterial calcification, generalized, of infancy, 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 65
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HGVS dbSNP
NM_006208.3(ENPP1):c.*1043A>G rs7754561
NM_006208.3(ENPP1):c.*1091A>C rs7754586
NM_006208.3(ENPP1):c.*1101G>T rs11154647
NM_006208.3(ENPP1):c.*112G>A rs1044548
NM_006208.3(ENPP1):c.*1137T>C rs11154648
NM_006208.3(ENPP1):c.*1157C>T rs7754859
NM_006208.3(ENPP1):c.*121G>C rs11964389
NM_006208.3(ENPP1):c.*1224A>G
NM_006208.3(ENPP1):c.*1236G>T rs11154649
NM_006208.3(ENPP1):c.*1299C>T rs11965061
NM_006208.3(ENPP1):c.*1348T>C rs9483349
NM_006208.3(ENPP1):c.*1350G>A rs9493120
NM_006208.3(ENPP1):c.*1539A>G rs9493121
NM_006208.3(ENPP1):c.*1559G>T rs551333973
NM_006208.3(ENPP1):c.*163C>T rs1044558
NM_006208.3(ENPP1):c.*1670T>C rs9493122
NM_006208.3(ENPP1):c.*1972G>C rs1931006
NM_006208.3(ENPP1):c.*2036A>G rs73778611
NM_006208.3(ENPP1):c.*2282G>A rs73778612
NM_006208.3(ENPP1):c.*2301A>G rs115728089
NM_006208.3(ENPP1):c.*2737C>T rs545095322
NM_006208.3(ENPP1):c.*2900G>T rs78495668
NM_006208.3(ENPP1):c.*3017C>T rs1931009
NM_006208.3(ENPP1):c.*3163C>T rs55670720
NM_006208.3(ENPP1):c.*3271C>G rs1510
NM_006208.3(ENPP1):c.*3511T>C rs9483350
NM_006208.3(ENPP1):c.*3594C>T rs140569538
NM_006208.3(ENPP1):c.*3615dup rs112718541
NM_006208.3(ENPP1):c.*3625G>A rs150482147
NM_006208.3(ENPP1):c.*3706G>A rs12205225
NM_006208.3(ENPP1):c.*3724C>T rs2327154
NM_006208.3(ENPP1):c.*3784T>C rs116417632
NM_006208.3(ENPP1):c.*3837T>C rs55725924
NM_006208.3(ENPP1):c.*3838G>A rs59958908
NM_006208.3(ENPP1):c.*3879A>G
NM_006208.3(ENPP1):c.*389G>A rs553
NM_006208.3(ENPP1):c.*400C>A
NM_006208.3(ENPP1):c.*4064T>C
NM_006208.3(ENPP1):c.*4248G>A rs150587148
NM_006208.3(ENPP1):c.*4571G>C rs574559068
NM_006208.3(ENPP1):c.*457T>A rs1044582
NM_006208.3(ENPP1):c.*4636C>T rs11963615
NM_006208.3(ENPP1):c.*4641A>G rs545401301
NM_006208.3(ENPP1):c.*477A>T
NM_006208.3(ENPP1):c.*563G>A rs1044586
NM_006208.3(ENPP1):c.*698_*699insA rs113083049
NM_006208.3(ENPP1):c.*699T>A rs34142005
NM_006208.3(ENPP1):c.*735A>G rs12212882
NM_006208.3(ENPP1):c.*772A>T rs34608785
NM_006208.3(ENPP1):c.*777C>T rs34836463
NM_006208.3(ENPP1):c.-13G>A rs535293574
NM_006208.3(ENPP1):c.1317A>G (p.Lys439=) rs9483347
NM_006208.3(ENPP1):c.1329T>C (p.Asp443=) rs113723070
NM_006208.3(ENPP1):c.1566-14T>C rs75272847
NM_006208.3(ENPP1):c.1831C>G (p.Leu611Val) rs79079368
NM_006208.3(ENPP1):c.2002G>A (p.Glu668Lys) rs115371819
NM_006208.3(ENPP1):c.2101-11del rs397832689
NM_006208.3(ENPP1):c.2106T>C (p.Ser702=) rs7750837
NM_006208.3(ENPP1):c.2124C>A (p.Phe708Leu) rs140521704
NM_006208.3(ENPP1):c.2320C>T (p.Arg774Cys) rs28933977
NM_006208.3(ENPP1):c.2335A>C (p.Thr779Pro) rs1805138
NM_006208.3(ENPP1):c.2661A>G (p.Ala887=) rs1804025
NM_006208.3(ENPP1):c.313+9G>T rs7773477
NM_006208.3(ENPP1):c.313+9GT[18] rs59956343
NM_006208.3(ENPP1):c.517A>C (p.Lys173Gln) rs1044498

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