List of variants in gene KLHL7 reported as likely benign for inborn disorder of amino acid metabolism

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001031710.3(KLHL7):c.*7A>G	rs112802878	0.01146
NM_001031710.3(KLHL7):c.*1052T>C	rs572464135	0.00143
NM_001031710.3(KLHL7):c.*98G>A	rs183472096	0.00143
NM_001031710.3(KLHL7):c.*898A>T	rs557309443	0.00054
NM_001031710.3(KLHL7):c.-206C>T	rs184270958	0.00046
NM_001031710.3(KLHL7):c.*1123A>C	rs752275483	0.00028
NM_001031710.3(KLHL7):c.*377G>A	rs142087633	0.00014
NM_001031710.3(KLHL7):c.-231G>C	rs556626844	0.00014
NM_001031710.3(KLHL7):c.-38G>A	rs200506606	0.00011
NM_001031710.3(KLHL7):c.-16A>G	rs563311203

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