Variants in gene KCNJ11 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.1143G>A (p.Lys381=)	rs8175351	0.01289
NM_000525.4(KCNJ11):c.678C>T (p.Pro226=)	rs74162102	0.00109

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