List of variants in gene KCNJ11 reported as benign for autosomal dominant hyperinsulinism due to Kir6.2 deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.1009G>A (p.Val337Ile)	rs5215	0.71351
NM_000525.4(KCNJ11):c.*441T>C	rs2285676	0.43747
NM_000525.4(KCNJ11):c.570C>T (p.Ala190=)	rs5218	0.22765
NM_000525.4(KCNJ11):c.808C>G (p.Leu270Val)	rs1800467	0.03859
NM_000525.4(KCNJ11):c.1143G>A (p.Lys381=)	rs8175351	0.01289
NM_000525.4(KCNJ11):c.*62G>A	rs5213

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