ClinVar Miner

List of variants reported as benign for Xeroderma pigmentosum variant type by Illumina Laboratory Services, Illumina

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ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_006502.3(POLH):c.*1858A>G rs9472090 0.19853
NM_006502.3(POLH):c.*290C>T rs6899628 0.12458
NM_006502.3(POLH):c.*2489C>T rs6922830 0.12414
NM_006502.3(POLH):c.1939A>T (p.Met647Leu) rs6941583 0.11871
NM_006502.3(POLH):c.*3847G>A rs145612937 0.05869
NM_006502.3(POLH):c.1434G>A (p.Thr478=) rs3734690 0.05476
NM_006502.3(POLH):c.*537C>T rs55704248 0.04781
NM_006502.3(POLH):c.*1129A>T rs28877272 0.03612
NM_006502.3(POLH):c.*50A>G rs1064260 0.03592
NM_006502.3(POLH):c.*1364T>A rs9333565 0.03584
NM_006502.3(POLH):c.*2975C>A rs112207298 0.03584
NM_006502.3(POLH):c.*5713T>C rs75658777 0.03578
NM_006502.3(POLH):c.*952C>T rs1141338 0.03574
NM_006502.3(POLH):c.*1110A>T rs112725367 0.03563
NM_006502.3(POLH):c.*1055A>T rs115129476 0.02324
NM_006502.3(POLH):c.*1679C>T rs113292021 0.02043
NM_006502.3(POLH):c.*2659T>C rs9462906 0.01968
NM_006502.3(POLH):c.1783A>G (p.Met595Val) rs9333555 0.01768
NM_006502.3(POLH):c.*693C>T rs9333558 0.01766
NM_006502.3(POLH):c.*5697G>A rs113410952 0.01678
NM_006502.3(POLH):c.*2499G>A rs147353387 0.01369
NM_006502.3(POLH):c.1751T>C (p.Leu584Pro) rs9333554 0.01368
NM_006502.3(POLH):c.*429G>A rs9333556 0.01366
NM_006502.3(POLH):c.*1179G>A rs9333561 0.01249
NM_006502.3(POLH):c.*3318G>A rs142340697 0.01222
NM_006502.3(POLH):c.*3611T>A rs73428626 0.00834
NM_006502.3(POLH):c.*371A>G rs59061501 0.00736
NM_006502.3(POLH):c.-117C>T rs56300149 0.00589
NM_006502.3(POLH):c.*1549C>T rs186059509 0.00525
NM_006502.3(POLH):c.-98A>C rs189835199 0.00524
NM_006502.3(POLH):c.986C>T (p.Thr329Ile) rs35675573 0.00520
NM_006502.3(POLH):c.*3088G>A rs373844625 0.00072
NM_006502.3(POLH):c.1433C>T (p.Thr478Met) rs9296419 0.00048
NM_006502.3(POLH):c.*3472A>G rs146828890 0.00043
NM_006502.3(POLH):c.*1940G>A rs527613993 0.00002
NM_006502.3(POLH):c.660+10A>C rs56056074 0.00001
NM_006502.3(POLH):c.*5630G>A rs116106873
NM_006502.3(POLH):c.*5933T>A rs567230078
NM_006502.3(POLH):c.*5934G>A rs534751786

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