List of variants in gene SLX4 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.2975G>A (p.Gly992Glu)	rs139287784	0.00049
NM_032444.4(SLX4):c.2585G>A (p.Arg862Gln)	rs143558209	0.00030
NM_032444.4(SLX4):c.3758C>T (p.Thr1253Ile)	rs202148391	0.00016
NM_032444.4(SLX4):c.4033C>T (p.Arg1345Cys)	rs200310925	0.00016
NM_032444.4(SLX4):c.4903A>G (p.Lys1635Glu)	rs140417509	0.00011
NM_032444.4(SLX4):c.3911T>G (p.Val1304Gly)	rs146837290	0.00009
NM_032444.4(SLX4):c.4856C>T (p.Pro1619Leu)	rs771200478	0.00005
NM_032444.4(SLX4):c.3235C>T (p.Pro1079Ser)	rs373231418	0.00004
NM_032444.4(SLX4):c.5404G>A (p.Asp1802Asn)	rs760435859	0.00004
NM_032444.4(SLX4):c.1520G>A (p.Arg507Lys)	rs762550449	0.00003
NM_032444.4(SLX4):c.5081C>T (p.Ala1694Val)	rs761226343	0.00001
NM_032444.4(SLX4):c.1331A>G (p.Glu444Gly)
NM_032444.4(SLX4):c.1951C>G (p.Pro651Ala)
NM_032444.4(SLX4):c.299C>A (p.Thr100Asn)	rs201163062
NM_032444.4(SLX4):c.3259A>C (p.Ser1087Arg)
NM_032444.4(SLX4):c.4804A>C (p.Thr1602Pro)	rs756198942
NM_032444.4(SLX4):c.5040G>C (p.Arg1680Ser)	rs199592185

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