List of variants in gene combination KCNQ5, KCNQ5-DT, LOC129996711 reported as uncertain significance for intellectual disability, autosomal dominant 46

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_019842.4(KCNQ5):c.49T>C (p.Trp17Arg)	rs971617867
NM_019842.4(KCNQ5):c.68CGG[7] (p.Ala26_Ala27dup)	rs568022266
NM_019842.4(KCNQ5):c.7C>A (p.Arg3Ser)	rs549110435
NM_019842.4(KCNQ5):c.8G>T (p.Arg3Leu)

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