List of variants in gene KCNJ11 reported as uncertain significance by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.584G>A (p.Arg195His)	rs5217	0.00131
NM_000525.4(KCNJ11):c.302C>A (p.Ala101Asp)	rs1014454531	0.00011
NM_000525.4(KCNJ11):c.-54C>T	rs1016780684	0.00010
NM_000525.4(KCNJ11):c.80G>A (p.Arg27His)	rs774714794	0.00004
NM_000525.4(KCNJ11):c.1093C>T (p.Arg365Cys)	rs758749160	0.00003
NM_000525.4(KCNJ11):c.1112G>A (p.Arg371His)	rs1233061680	0.00003
NM_000525.4(KCNJ11):c.575G>A (p.Arg192His)	rs750778014	0.00003
NM_000525.4(KCNJ11):c.853G>A (p.Val285Ile)	rs149667199	0.00003
NM_000525.4(KCNJ11):c.1040G>A (p.Arg347His)	rs771797701	0.00002
NM_000525.4(KCNJ11):c.292G>A (p.Gly98Ser)	rs1554901851	0.00002
NM_000525.4(KCNJ11):c.970G>A (p.Gly324Arg)	rs1193170151	0.00002
NM_000525.4(KCNJ11):c.1016T>G (p.Val339Gly)	rs138125678	0.00001
NM_000525.4(KCNJ11):c.1094G>A (p.Arg365His)	rs750689750	0.00001
NM_000525.4(KCNJ11):c.407G>A (p.Arg136His)	rs1479483693	0.00001
NM_000525.4(KCNJ11):c.463G>A (p.Val155Met)	rs587783668	0.00001
NM_000525.4(KCNJ11):c.527G>A (p.Arg176His)	rs1266231295	0.00001
NM_000525.4(KCNJ11):c.79C>T (p.Arg27Cys)	rs752507753	0.00001
NM_000525.3(KCNJ11):c.1138_1143dup (p.Lys381_Phe382insProLys)	rs1440128889
NM_000525.4(KCNJ11):c.-135_-134insCT	rs1554901983
NM_000525.4(KCNJ11):c.119G>A (p.Gly40Asp)	rs1001873841
NM_000525.4(KCNJ11):c.264G>T (p.Met88Ile)	rs1554901866
NM_000525.4(KCNJ11):c.617G>T (p.Arg206Leu)	rs1554901747
NM_000525.4(KCNJ11):c.662G>A (p.Arg221His)	rs768909861
NM_000525.4(KCNJ11):c.797C>T (p.Pro266Leu)	rs1554901679
NM_000525.4(KCNJ11):c.841_843del (p.Leu281del)	rs1554901658

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