List of variants in gene SLX4 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu)	rs149126845	0.00087
NM_032444.4(SLX4):c.4261A>T (p.Ile1421Phe)	rs141567438	0.00069
NM_032444.4(SLX4):c.2681T>G (p.Val894Gly)	rs145137472	0.00036
NM_032444.4(SLX4):c.4590G>A (p.Met1530Ile)	rs147315419	0.00024
NM_032444.4(SLX4):c.2023G>A (p.Gly675Arg)	rs767473953	0.00004
NM_032444.4(SLX4):c.5404G>A (p.Asp1802Asn)	rs760435859	0.00004
NM_032444.4(SLX4):c.1222C>T (p.Arg408Trp)	rs758029323	0.00003
NM_032444.4(SLX4):c.3089C>T (p.Pro1030Leu)	rs774562724	0.00003
NM_032444.4(SLX4):c.2021T>G (p.Leu674Arg)	rs889646690	0.00001
NM_032444.4(SLX4):c.2321C>G (p.Ala774Gly)	rs376389326	0.00001
NM_032444.4(SLX4):c.1468C>T (p.Leu490Phe)
NM_032444.4(SLX4):c.1795G>A (p.Gly599Ser)
NM_032444.4(SLX4):c.3680G>A (p.Gly1227Asp)	rs192144067
NM_032444.4(SLX4):c.873G>C (p.Lys291Asn)	rs751904877

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