List of variants in gene DRD4 reported as uncertain significance for Hereditary attention deficit-hyperactivity disorder

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000797.4(DRD4):c.1058-32G>C	rs1870724	0.29133
NM_000797.4(DRD4):c.860A>C (p.Gln287Pro)	rs769762387	0.11156
NM_000797.4(DRD4):c.922T>C (p.Ser308Pro)	rs534428944	0.00019
NM_000797.4(DRD4):c.-11C>T	rs146680769
NM_000797.4(DRD4):c.485T>G (p.Leu162Arg)	rs1370276664
NM_000797.4(DRD4):c.52_62del (p.Pro18fs)	rs1279080134
NM_000797.4(DRD4):c.759_806dup (p.Pro270_Arg271insGlnAspProCysGlyProAspCysAlaProProAlaProGlyLeuPro)	rs1564913700
NM_000797.4(DRD4):c.807T>C (p.Leu269=)	rs866686536
NM_000797.4(DRD4):c.812G>A (p.Arg271Gln)	rs767239460
NM_000797.4(DRD4):c.815G>A (p.Gly272Asp)	rs749976218
NM_000797.4(DRD4):c.816T>C (p.Gly272=)	rs1256049181
NM_000797.4(DRD4):c.850A>G (p.Ser284Gly)	rs34662058
NM_000797.4(DRD4):c.869_870insTGG (p.Gly291_Pro292insGly)	rs1360339521
NM_000797.4(DRD4):c.925A>G (p.Asn309Asp)	rs781463894
NM_000797.4(DRD4):c.933T>G (p.Ala311=)	rs547842677

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