List of variants in gene SARS2 reported as likely benign for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017827.4(SARS2):c.*99T>G	rs74399089	0.01201
NM_017827.4(SARS2):c.273G>A (p.Ser91=)	rs144229840	0.00672
NM_017827.4(SARS2):c.364-14C>T	rs150151686	0.00412
NM_017827.4(SARS2):c.963-17T>C	rs201465773	0.00136
NM_017827.4(SARS2):c.696C>T (p.Arg232=)	rs35389151	0.00118
NM_017827.4(SARS2):c.576C>T (p.Val192=)	rs150249937	0.00048
NM_017827.4(SARS2):c.1348-19G>A	rs540813245	0.00009
NM_017827.4(SARS2):c.540C>T (p.Val180=)	rs371250326	0.00006
NM_017827.4(SARS2):c.*116C>T	rs563670346	0.00004
NM_017827.4(SARS2):c.795C>T (p.Arg265=)	rs372151812	0.00003
NM_017827.4(SARS2):c.534+9C>T	rs200404554	0.00002
NM_017827.4(SARS2):c.916+10TG[2]	rs60352446

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