List of variants in gene SLC7A14 reported as uncertain significance for Retinitis pigmentosa 68

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020949.3(SLC7A14):c.1391G>T (p.Cys464Phe)	rs79668755	0.00044
NM_020949.3(SLC7A14):c.1246C>T (p.Leu416Phe)	rs753129566	0.00021
NM_020949.3(SLC7A14):c.1168G>C (p.Val390Leu)	rs142416793

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