ClinVar Miner

List of variants in gene SARS2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_017827.4(SARS2):c.1160+4T>C rs7508411 0.73282
NM_017827.4(SARS2):c.1160+278A>G rs9749516 0.72773
NM_017827.4(SARS2):c.808-66G>T rs11083489 0.72763
NM_017827.4(SARS2):c.963-40G>C rs4803034 0.72763
NM_017827.4(SARS2):c.759+283T>C rs2099339 0.46664
NM_017827.4(SARS2):c.1160+130G>A rs2288855 0.46589
NM_017827.4(SARS2):c.*79G>C rs9403 0.46106
NM_017827.4(SARS2):c.1161-60G>T rs4801945 0.46026
NM_017827.4(SARS2):c.590-197G>C rs12460327 0.26071
NM_017827.4(SARS2):c.364-255G>A rs12977011 0.20764
NM_017827.4(SARS2):c.268-27T>A rs4803046 0.20730
NM_017827.4(SARS2):c.268-26C>A rs4803045 0.20722
NM_017827.4(SARS2):c.760-184G>A rs12459197 0.18301
NM_017827.4(SARS2):c.1413+39C>T rs11670675 0.17484
NM_017827.4(SARS2):c.321G>A (p.Glu107=) rs11544093 0.14659
NM_017827.4(SARS2):c.267+308A>G rs7260466 0.14652
NM_017827.4(SARS2):c.1161-239T>G rs59785584 0.07044
NM_017827.4(SARS2):c.1254+36A>C rs73930228 0.05897
NM_017827.4(SARS2):c.1161-202C>T rs73930229 0.05830
NM_017827.4(SARS2):c.363+130G>A rs112422782 0.04782
NM_017827.4(SARS2):c.363+70C>A rs73930233 0.04037
NM_017827.4(SARS2):c.364-231G>A rs73930231 0.03683
NM_017827.4(SARS2):c.1414-39G>A rs10407222 0.02408
NM_017827.4(SARS2):c.273G>A (p.Ser91=) rs144229840 0.00672
NM_017827.4(SARS2):c.310C>T (p.Arg104Trp) rs144760517 0.00518
NM_017827.4(SARS2):c.531C>T (p.Asp177=) rs116583253 0.00416
NM_017827.4(SARS2):c.364-14C>T rs150151686 0.00412
NM_017827.4(SARS2):c.390G>A (p.Gln130=) rs61736057 0.00233
NM_017827.4(SARS2):c.501G>A (p.Ala167=) rs140304897 0.00063
NM_017827.4(SARS2):c.576C>T (p.Val192=) rs150249937 0.00048
NM_017827.4(SARS2):c.590-5T>A rs370612303 0.00035
NM_017827.4(SARS2):c.1161-275dup rs11450388
NM_017827.4(SARS2):c.1530_1538dup (p.Leu511_Gly513dup) rs551671819
NM_017827.4(SARS2):c.393+112dup rs59946162
NM_017827.4(SARS2):c.393+149del rs375344827
NM_017827.4(SARS2):c.394-138C>T rs10412886
NM_017827.4(SARS2):c.916+10TG[2] rs60352446

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