List of variants in gene SARS2 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_017827.4(SARS2):c.352C>T (p.Arg118Trp)	rs147412052	0.00057
NM_017827.4(SARS2):c.1292G>A (p.Arg431His)	rs146193366	0.00010
NM_017827.4(SARS2):c.1501A>G (p.Ile501Val)	rs776562420	0.00009
NM_017827.4(SARS2):c.988C>T (p.Arg330Trp)	rs781367675	0.00009
NM_017827.4(SARS2):c.637G>A (p.Asp213Asn)	rs151116675	0.00008
NM_017827.4(SARS2):c.1291C>T (p.Arg431Cys)	rs752872984	0.00006
NM_017827.4(SARS2):c.796G>A (p.Gly266Arg)	rs767412508	0.00002
NM_017827.4(SARS2):c.1255-3C>T
NM_017827.4(SARS2):c.1376G>A (p.Arg459His)	rs1064796265
NM_017827.4(SARS2):c.427C>G (p.Arg143Gly)
NM_017827.4(SARS2):c.500C>T (p.Ala167Val)
NM_017827.4(SARS2):c.600C>G (p.Phe200Leu)
NM_017827.4(SARS2):c.603A>G (p.Gln201=)
NM_017827.4(SARS2):c.634C>G (p.Leu212Val)	rs863224196
NM_017827.4(SARS2):c.650A>C (p.Gln217Pro)
NM_017827.4(SARS2):c.868C>T (p.Arg290Cys)
NM_017827.4(SARS2):c.929A>G (p.Asp310Gly)
NM_017827.4(SARS2):c.950A>G (p.Asp317Gly)

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