List of variants in gene KLHL7 reported as likely pathogenic for perceptual disorders

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001031710.3(KLHL7):c.422T>C (p.Val141Ala)	rs1554286384
NM_001031710.3(KLHL7):c.433A>G (p.Asn145Asp)	rs1182983579
NM_001031710.3(KLHL7):c.433A>T (p.Asn145Tyr)	rs1182983579
NM_001031710.3(KLHL7):c.458C>T (p.Ala153Val)	rs137853113
NM_001031710.3(KLHL7):c.472T>C (p.Cys158Arg)	rs1784156837
NM_001031710.3(KLHL7):c.569dup (p.Thr191fs)
NM_001031710.3(KLHL7):c.576TCT[1] (p.Leu194del)
NM_001031710.3(KLHL7):c.618+1G>A	rs1554289078

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