List of variants in gene SLX4 reported as uncertain significance by Revvity Omics, Revvity

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.2305G>C (p.Glu769Gln)	rs150712805	0.00119
NM_032444.4(SLX4):c.2654C>T (p.Pro885Leu)	rs147492092	0.00036
NM_032444.4(SLX4):c.2609C>T (p.Ala870Val)	rs149584080	0.00031
NM_032444.4(SLX4):c.2585G>A (p.Arg862Gln)	rs143558209	0.00030
NM_032444.4(SLX4):c.5212G>T (p.Gly1738Trp)	rs556217576	0.00025
NM_032444.4(SLX4):c.832C>T (p.Arg278Trp)	rs141597706	0.00014
NM_032444.4(SLX4):c.4403G>A (p.Arg1468His)	rs574214196	0.00008
NM_032444.4(SLX4):c.3101G>A (p.Arg1034His)	rs150453226	0.00006
NM_032444.4(SLX4):c.5072A>G (p.Asn1691Ser)	rs551385115	0.00006
NM_032444.4(SLX4):c.145G>A (p.Glu49Lys)	rs139757085	0.00005
NM_032444.4(SLX4):c.3136C>T (p.Arg1046Cys)	rs140529288	0.00005
NM_032444.4(SLX4):c.3746G>A (p.Ser1249Asn)	rs372991604	0.00004
NM_032444.4(SLX4):c.1045A>G (p.Arg349Gly)
NM_032444.4(SLX4):c.5195G>C (p.Gly1732Ala)
NM_032444.4(SLX4):c.678C>A (p.His226Gln)	rs28516461

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