List of variants in gene KCNJ1 reported as likely pathogenic for not provided

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_153766.3(KCNJ1):c.875G>A (p.Arg292Gln)	rs373198476	0.00010
NM_153766.3(KCNJ1):c.601C>T (p.Leu201Phe)	rs200320892	0.00004
NM_153766.3(KCNJ1):c.955C>T (p.Arg319Ter)	rs377205432	0.00003
NM_153766.3(KCNJ1):c.867C>A (p.Cys289Ter)	rs746509804	0.00001
NM_153766.3(KCNJ1):c.240G>T (p.Trp80Cys)
NM_153766.3(KCNJ1):c.535G>A (p.Ala179Thr)	rs104894253
NM_153766.3(KCNJ1):c.600C>A (p.Ser200Arg)
NM_153766.3(KCNJ1):c.751C>T (p.His251Tyr)
NM_153766.3(KCNJ1):c.76A>G (p.Lys26Glu)
NM_153766.3(KCNJ1):c.884A>G (p.Tyr295Cys)

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