Variants in gene KCNJ11 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.1009G>A (p.Val337Ile)	rs5215	0.70936
NM_000525.4(KCNJ11):c.*215C>T	rs5210	0.44390
NM_000525.4(KCNJ11):c.570C>T (p.Ala190=)	rs5218	0.23002
NM_000525.4(KCNJ11):c.808C>G (p.Leu270Val)	rs1800467	0.03694
NM_000525.4(KCNJ11):c.801C>G (p.Leu267=)	rs5216	0.01521
NM_000525.4(KCNJ11):c.*766G>A	rs193101892	0.00683
NM_000525.4(KCNJ11):c.1095C>T (p.Arg365=)	rs143276279	0.00167
NM_000525.4(KCNJ11):c.584G>A (p.Arg195His)	rs5217	0.00122
NM_000525.4(KCNJ11):c.678C>T (p.Pro226=)	rs74162102	0.00101
NM_000525.4(KCNJ11):c.843C>T (p.Leu281=)	rs116392938	0.00029

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