List of variants in gene RPS4X reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001007.5(RPS4X):c.390T>G (p.Phe130Leu)	rs759573596	0.00005
NM_001007.5(RPS4X):c.157A>C (p.Lys53Gln)	rs772048739	0.00004
NM_001007.5(RPS4X):c.124C>T (p.Leu42Phe)	rs747294461
NM_001007.5(RPS4X):c.392T>C (p.Val131Ala)
NM_001007.5(RPS4X):c.434G>A (p.Arg145His)
NM_001007.5(RPS4X):c.599G>A (p.Arg200Lys)
NM_001007.5(RPS4X):c.7C>T (p.Arg3Cys)	rs1179468202

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