List of variants in gene KCNJ11 reported as pathogenic for digestive system disorder

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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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.844G>A (p.Glu282Lys)	rs267607196	0.00003
NM_000525.4(KCNJ11):c.101G>A (p.Arg34His)	rs141145502	0.00001
NM_000525.4(KCNJ11):c.406C>T (p.Arg136Cys)	rs766891274	0.00001
NM_000525.4(KCNJ11):c.761C>T (p.Pro254Leu)	rs104894237	0.00001
NM_000525.4(KCNJ11):c.776A>G (p.His259Arg)	rs104894248	0.00001
NM_000525.4(KCNJ11):c.881C>T (p.Thr294Met)	rs780957825	0.00001
NM_000525.4(KCNJ11):c.902G>A (p.Arg301His)	rs74339576	0.00001
NM_000525.4(KCNJ11):c.-134G>T	rs387906398
NM_000525.4(KCNJ11):c.124T>C (p.Cys42Arg)	rs80356610
NM_000525.4(KCNJ11):c.149G>A (p.Arg50Gln)	rs80356611
NM_000525.4(KCNJ11):c.149G>C (p.Arg50Pro)	rs80356611
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.179T>A (p.Phe60Tyr)	rs387906783
NM_000525.4(KCNJ11):c.368dup (p.Ser124fs)	rs1554901822
NM_000525.4(KCNJ11):c.36C>A (p.Tyr12Ter)	rs104894236
NM_000525.4(KCNJ11):c.405dup (p.Arg136fs)	rs557160758
NM_000525.4(KCNJ11):c.440T>C (p.Leu147Pro)	rs28936678
NM_000525.4(KCNJ11):c.466G>A (p.Gly156Arg)	rs1404429785
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.601C>T (p.Arg201Cys)	rs80356625
NM_000525.4(KCNJ11):c.602G>A (p.Arg201His)	rs80356624
NM_000525.4(KCNJ11):c.679G>A (p.Glu227Lys)	rs587783672
NM_000525.4(KCNJ11):c.685G>A (p.Glu229Lys)	rs587783673
NM_000525.4(KCNJ11):c.889ACC[1] (p.Thr298del)	rs1953574433
NM_000525.4(KCNJ11):c.964G>A (p.Glu322Lys)	rs193929355
NM_000525.4(KCNJ11):c.967dup (p.Asp323fs)	rs1554901596
NM_000525.4(KCNJ11):c.988T>C (p.Tyr330His)	rs587783675

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