ClinVar Miner

List of variants in gene RRM2B reported as benign for not provided

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_015713.5(RRM2B):c.49-25C>T rs3735722 0.11798
NM_015713.5(RRM2B):c.*732A>G rs16869269 0.11676
NM_015713.5(RRM2B):c.*866T>G rs29000286 0.11598
NM_015713.5(RRM2B):c.*1673T>G rs16918482 0.11578
NM_015713.5(RRM2B):c.789+303_789+304insG rs111489051 0.10846
NM_015713.5(RRM2B):c.48+64G>A rs28999669 0.10515
NM_015713.5(RRM2B):c.204+156G>A rs2015704 0.10275
NM_015713.5(RRM2B):c.551-156G>T rs13249865 0.10054
NM_015713.5(RRM2B):c.*1488G>C rs1265116 0.10011
NM_015713.5(RRM2B):c.48+215dup rs5893603 0.07499
NM_015713.5(RRM2B):c.48+125G>A rs1037699 0.07464
NM_015713.5(RRM2B):c.322-288A>G rs28928571 0.06879
NM_015713.5(RRM2B):c.49-67T>G rs16869295 0.06853
NM_015713.5(RRM2B):c.321+218G>A rs7841131 0.06837
NM_015713.5(RRM2B):c.*998A>G rs3907099 0.06791
NM_015713.5(RRM2B):c.*3593G>A rs29000294 0.06703
NM_015713.5(RRM2B):c.*1277A>T rs5005121 0.06698
NM_015713.5(RRM2B):c.*2666T>C rs3735721 0.06688
NM_015713.5(RRM2B):c.48+280C>G rs1037700 0.06112
NM_015713.5(RRM2B):c.*3527G>A rs1052071 0.05633
NM_015713.5(RRM2B):c.*3463C>T rs1052069 0.05623
NM_015713.5(RRM2B):c.205-335A>G rs28999706 0.05464
NM_015713.5(RRM2B):c.790-106T>G rs29000274 0.05427
NM_015713.5(RRM2B):c.*1121T>C rs4102401 0.04883
NM_015713.5(RRM2B):c.*3395C>G rs11575866 0.04883
NM_015713.5(RRM2B):c.*2879A>G rs3204695 0.04874
NM_015713.5(RRM2B):c.322-37A>G rs28928572 0.04041
NM_015713.5(RRM2B):c.207C>T (p.Val69=) rs28999710 0.02727
NM_015713.5(RRM2B):c.904-248T>G rs73283330 0.01869
NM_015713.5(RRM2B):c.*2136G>A rs139212686 0.01300
NM_015713.5(RRM2B):c.48+273G>T rs149523343 0.00928
NM_015713.5(RRM2B):c.48+48C>T rs201028777 0.00142
NM_015713.5(RRM2B):c.685-20A>T rs142382577 0.00104
NM_015713.5(RRM2B):c.551-18C>T rs72554100 0.00062
NM_015713.5(RRM2B):c.*1601A>G rs140164634 0.00048
NM_015713.5(RRM2B):c.790-8C>A rs376542259 0.00014
NM_015713.5(RRM2B):c.48+118C>T rs779614160 0.00004
NC_000008.11:g.102238956TCCGCTGG[3] rs28999668
NM_015713.5(RRM2B):c.*2675A>G rs3735720
NM_015713.5(RRM2B):c.204+263dup rs1250881056
NM_015713.5(RRM2B):c.204+280del rs1250881056
NM_015713.5(RRM2B):c.205-275del rs11333663
NM_015713.5(RRM2B):c.205-310TA[10] rs28999707
NM_015713.5(RRM2B):c.322-25_322-18dup rs566628697
NM_015713.5(RRM2B):c.456-202G>A rs117329782
NM_015713.5(RRM2B):c.551-11_551-10del rs771845744
NM_015713.5(RRM2B):c.684+281G>A rs3018505
NM_015713.5(RRM2B):c.684+72dup rs573218615
NM_015713.5(RRM2B):c.790-66_790-63del rs29000276

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