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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_019842.4(KCNQ5):c.292A>G (p.Ser98Gly)	rs2154471235
NM_019842.4(KCNQ5):c.326G>T (p.Arg109Leu)	rs2154471240
NM_019842.4(KCNQ5):c.359A>C (p.Glu120Ala)

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