List of variants in gene QDPR reported as uncertain significance for Inborn genetic diseases

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000320.3(QDPR):c.425A>G (p.Asp142Gly)	rs138542030	0.00014
NM_000320.3(QDPR):c.274G>A (p.Gly92Arg)	rs757963200	0.00007
NM_000320.3(QDPR):c.728A>G (p.Tyr243Cys)	rs565356844	0.00005
NM_000320.3(QDPR):c.409G>A (p.Ala137Thr)	rs778631854	0.00003
NM_000320.3(QDPR):c.385G>A (p.Gly129Arg)	rs763771086	0.00002
NM_000320.3(QDPR):c.254G>C (p.Cys85Ser)
NM_000320.3(QDPR):c.308A>G (p.Asn103Ser)	rs1248495029
NM_000320.3(QDPR):c.328C>A (p.Gln110Lys)
NM_000320.3(QDPR):c.463G>A (p.Gly155Ser)	rs2474658462
NM_000320.3(QDPR):c.658A>C (p.Asn220His)	rs2474652102
NM_000320.3(QDPR):c.691G>A (p.Val231Ile)

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