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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.100C>T (p.Arg34Cys)	rs954727530	0.00001
NM_000525.4(KCNJ11):c.101G>A (p.Arg34His)	rs141145502	0.00001
NM_000525.4(KCNJ11):c.616C>T (p.Arg206Cys)	rs775204908	0.00001
NM_000525.4(KCNJ11):c.776A>G (p.His259Arg)	rs104894248	0.00001
NM_000525.4(KCNJ11):c.157G>A (p.Gly53Ser)	rs80356613
NM_000525.4(KCNJ11):c.405dup (p.Arg136fs)	rs557160758
NM_000525.4(KCNJ11):c.556C>G (p.His186Asp)	rs2133380076

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