List of variants in gene SLX4 reported as uncertain significance by Gharavi Laboratory, Columbia University

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_032444.4(SLX4):c.2977G>T (p.Glu993Ter)	rs1567170533
NM_032444.4(SLX4):c.3331_3332insTA (p.Asn1111fs)	rs1567170211
NM_032444.4(SLX4):c.4823C>G (p.Ser1608Ter)	rs200628199
NM_032444.4(SLX4):c.5153+1G>A	rs1567166275

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