List of variants in gene KCNJ11 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.941G>A (p.Arg314His)	rs145935651	0.00011
NM_000525.4(KCNJ11):c.-54C>T	rs1016780684	0.00010
NM_000525.4(KCNJ11):c.*218G>T	rs886048039	0.00009
NM_000525.4(KCNJ11):c.934G>A (p.Gly312Ser)	rs72554079	0.00008
NM_000525.4(KCNJ11):c.47G>A (p.Arg16His)	rs770609243	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.353C>T (p.Ser118Leu)	rs756424776	0.00002
NM_000525.4(KCNJ11):c.1016T>G (p.Val339Gly)	rs138125678	0.00001
NM_000525.4(KCNJ11):c.1044G>C (p.Gln348His)	rs745379486	0.00001
NM_000525.4(KCNJ11):c.1106G>T (p.Arg369Leu)	rs114613745	0.00001
NM_000525.4(KCNJ11):c.411G>A (p.Met137Ile)	rs371977895	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_000525.3(KCNJ11):c.1138_1143dup (p.Lys381_Phe382insProLys)	rs1440128889
NM_000525.4(KCNJ11):c.-150G>A	rs886048043
NM_000525.4(KCNJ11):c.10C>T (p.Arg4Cys)	rs543286136
NM_000525.4(KCNJ11):c.662G>A (p.Arg221His)	rs768909861
NM_000525.4(KCNJ11):c.905C>T (p.Thr302Ile)	rs761575495
NM_000525.4(KCNJ11):c.973C>A (p.Arg325Ser)	rs550315112

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