List of variants in gene STAG2 reported as uncertain significance for Inborn genetic diseases

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001042750.2(STAG2):c.2000G>A (p.Arg667Gln)
NM_001042750.2(STAG2):c.2051C>G (p.Ala684Gly)
NM_001042750.2(STAG2):c.2549A>T (p.Asp850Val)
NM_001042750.2(STAG2):c.3337C>T (p.Pro1113Ser)	rs1556571924
NM_001042750.2(STAG2):c.631C>G (p.Gln211Glu)	rs2057841126
NM_001042750.2(STAG2):c.884A>G (p.His295Arg)	rs2057961508
NM_001042750.2(STAG2):c.98A>G (p.Lys33Arg)

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