List of variants in gene KCNJ10 reported as uncertain significance for not specified

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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_002241.5(KCNJ10):c.735C>G (p.Asp245Glu)	rs146426296	0.00155
NM_002241.5(KCNJ10):c.136G>A (p.Asp46Asn)	rs141553756	0.00146
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His)	rs146396982	0.00034
NM_002241.5(KCNJ10):c.301C>A (p.Pro101Thr)	rs375361490	0.00011
NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys)	rs137853074	0.00008
NM_002241.5(KCNJ10):c.10G>A (p.Val4Ile)	rs144428351	0.00003
NM_002241.5(KCNJ10):c.274G>T (p.Ala92Ser)	rs1314505994	0.00001
NM_002241.5(KCNJ10):c.652C>T (p.Leu218Phe)	rs558502886	0.00001
NM_002241.5(KCNJ10):c.300C>A (p.Asp100Glu)	rs139069413
NM_002241.5(KCNJ10):c.922G>C (p.Gly308Arg)	rs1557967657

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