List of variants in gene SLX4 reported as uncertain significance by Mendelics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.467C>A (p.Thr156Lys)	rs144614070	0.00038
NM_032444.4(SLX4):c.2654C>T (p.Pro885Leu)	rs147492092	0.00036
NM_032444.4(SLX4):c.2941G>A (p.Gly981Arg)	rs546628836	0.00006
NM_032444.4(SLX4):c.1547C>T (p.Ala516Val)	rs199683722	0.00003
NM_032444.4(SLX4):c.4021A>G (p.Arg1341Gly)	rs747230215	0.00002
NM_032444.4(SLX4):c.2878A>T (p.Ser960Cys)	rs772190416	0.00001
NM_032444.4(SLX4):c.1186C>G (p.Leu396Val)	rs1596528058
NM_032444.4(SLX4):c.3607C>G (p.Pro1203Ala)	rs745508761
NM_032444.4(SLX4):c.3830G>A (p.Ser1277Asn)	rs1596520868
NM_032444.4(SLX4):c.421G>T (p.Gly141Trp)	rs137976282

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