ClinVar Miner

List of variants in gene RPS20 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001146227.3(RPS20):c.*35+247T>C rs2976050 0.27904
NM_001023.4(RPS20):c.103+88G>C rs2976045 0.25498
NM_001023.4(RPS20):c.4-19T>C rs2976044 0.25239
NM_001023.4(RPS20):c.195A>G (p.Thr65=) rs1050403 0.15735
NM_001023.4(RPS20):c.-6A>G rs1128142 0.09799
NM_001023.4(RPS20):c.178-181G>C rs77156325 0.04433
NM_001146227.3(RPS20):c.*35+178G>C rs4576403 0.04432
NM_001146227.3(RPS20):c.*35+220C>T rs4276661 0.04426
NM_001023.4(RPS20):c.177+180A>G rs7841318 0.03469
NM_001023.4(RPS20):c.4-11T>C rs113118429 0.02567
NM_001023.4(RPS20):c.4-90G>A rs73592343 0.02357
NM_001023.4(RPS20):c.-117G>C rs73679777 0.02356
NM_001023.4(RPS20):c.177+76G>C rs16920302 0.02356
NM_001146227.3(RPS20):c.343T>C (p.Ser115Pro) rs79444047 0.02024
NM_001023.3(RPS20):c.*236G>C rs116472667 0.02023
NM_001146227.3(RPS20):c.334-187G>A rs116634965 0.02023
NM_001146227.3(RPS20):c.*35G>A rs150975205 0.00985
NM_001023.4(RPS20):c.177+19G>A rs143312326 0.00105
NM_001023.4(RPS20):c.3+13T>G rs755111939 0.00024
NM_001023.4(RPS20):c.271T>C (p.Leu91=) rs768823942 0.00022
NM_001023.4(RPS20):c.228G>A (p.Thr76=) rs540124601 0.00011
NM_001023.4(RPS20):c.177+19del
NM_001023.4(RPS20):c.177+19dup rs34275230
NM_001023.4(RPS20):c.3+57C>G rs79460063
NM_001023.4(RPS20):c.4-3T>C rs7841901

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