List of variants in gene PDE6B reported as benign for inborn disorder of amino acid metabolism

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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_000283.4(PDE6B):c.958G>A (p.Val320Ile)	rs10902758	0.99926
NM_000283.4(PDE6B):c.*12A>G	rs28675771	0.58217
NM_000283.4(PDE6B):c.*191C>A	rs111449765	0.02743
NM_000283.4(PDE6B):c.373C>G (p.Pro125Ala)	rs28414606	0.02568
NM_000283.4(PDE6B):c.384C>T (p.Ser128=)	rs28510278	0.02567
NM_000283.4(PDE6B):c.655T>C (p.Tyr219His)	rs62295357	0.00465
NM_000283.4(PDE6B):c.928-9_940dup	rs539992414

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