List of variants in gene KCNJ11 reported as not provided

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.47G>A (p.Arg16His)	rs770609243	0.00003
NM_000525.4(KCNJ11):c.1001G>A (p.Gly334Asp)	rs193929358
NM_000525.4(KCNJ11):c.103T>C (p.Phe35Leu)	rs193929333
NM_000525.4(KCNJ11):c.103T>G (p.Phe35Val)	rs193929333
NM_000525.4(KCNJ11):c.124T>C (p.Cys42Arg)	rs80356610
NM_000525.4(KCNJ11):c.149G>C (p.Arg50Pro)	rs80356611
NM_000525.4(KCNJ11):c.155A>G (p.Gln52Arg)	rs193929337
NM_000525.4(KCNJ11):c.157G>A (p.Gly53Ser)	rs80356613
NM_000525.4(KCNJ11):c.157G>C (p.Gly53Arg)	rs80356613
NM_000525.4(KCNJ11):c.158G>A (p.Gly53Asp)	rs80356615
NM_000525.4(KCNJ11):c.175G>A (p.Val59Met)	rs80356616
NM_000525.4(KCNJ11):c.176T>G (p.Val59Gly)	rs80356617
NM_000525.4(KCNJ11):c.497G>A (p.Cys166Tyr)	rs80356618
NM_000525.4(KCNJ11):c.497G>T (p.Cys166Phe)	rs80356618
NM_000525.4(KCNJ11):c.499A>C (p.Ile167Leu)	rs80356620
NM_000525.4(KCNJ11):c.509A>G (p.Lys170Arg)	rs80356621
NM_000525.4(KCNJ11):c.510G>C (p.Lys170Asn)	rs80356622
NM_000525.4(KCNJ11):c.544A>G (p.Ile182Val)	rs193929348
NM_000525.4(KCNJ11):c.601C>T (p.Arg201Cys)	rs80356625
NM_000525.4(KCNJ11):c.602G>A (p.Arg201His)	rs80356624
NM_000525.4(KCNJ11):c.602G>T (p.Arg201Leu)	rs80356624
NM_000525.4(KCNJ11):c.755T>C (p.Val252Ala)	rs193929352
NM_000525.4(KCNJ11):c.886A>C (p.Ile296Leu)	rs193929353
NM_000525.4(KCNJ11):c.886A>G (p.Ile296Val)	rs193929353
NM_000525.4(KCNJ11):c.964G>A (p.Glu322Lys)	rs193929355
NM_000525.4(KCNJ11):c.989A>G (p.Tyr330Cys)	rs193929356
NM_000525.4(KCNJ11):c.997T>A (p.Phe333Ile)	rs193929357

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