List of variants in gene KCNJ1 reported as likely benign by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_153766.3(KCNJ1):c.-21-2316G>A	rs148983839	0.01182
NM_153766.3(KCNJ1):c.-21-1973A>G	rs75594566	0.00694
NM_153766.3(KCNJ1):c.*16G>A	rs3181542	0.00550
NM_153766.3(KCNJ1):c.*96del	rs142894410
NM_153766.3(KCNJ1):c.-21-2532T>C	rs6590353

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