List of variants in gene SUMF1 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_182760.4(SUMF1):c.797C>T (p.Pro266Leu)	rs763243827	0.00011
NM_182760.4(SUMF1):c.1000T>C (p.Tyr334His)
NM_182760.4(SUMF1):c.866A>G (p.Tyr289Cys)	rs772860745
NM_182760.4(SUMF1):c.891C>G (p.Asn297Lys)	rs143754187

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