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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.130G>A (p.Val44Met)	rs1282255458	0.00001
NM_000525.4(KCNJ11):c.160C>T (p.Arg54Cys)	rs375848765	0.00001
NM_000525.4(KCNJ11):c.185C>T (p.Thr62Met)	rs1057518775	0.00001
NM_000525.4(KCNJ11):c.874G>A (p.Glu292Lys)	rs1174593640	0.00001
NM_000525.4(KCNJ11):c.148C>T (p.Arg50Trp)
NM_000525.4(KCNJ11):c.490C>T (p.Leu164Phe)	rs1554901796
NM_000525.4(KCNJ11):c.515C>T (p.Ala172Val)	rs1426834688
NM_000525.4(KCNJ11):c.536A>C (p.Glu179Ala)	rs587783671
NM_000525.4(KCNJ11):c.556C>T (p.His186Tyr)

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