List of variants in gene KCNJ10 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.179T>C (p.Ile60Thr)	rs759993423	0.00001
NM_002241.5(KCNJ10):c.511C>T (p.Arg171Trp)	rs769666695	0.00001
NM_002241.5(KCNJ10):c.487G>T (p.Gly163Cys)

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