"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "KCNJ10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 205824	NM_002241.5(KCNJ10):c.1061A>G (p.Lys354Arg)	KCNJ10 (K354R)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 4 +5 more	GConflicting classifications of pathogenicity
Select item 7470	NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys)	KCNJ10 (R348C)	Single nucleotide variant (missense variant)	KCNJ10-related disorder +3 more	GUncertain significance
Select item 1163174	NM_002241.5(KCNJ10):c.1031A>G (p.Asp344Gly)	KCNJ10 (D344G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1163175	NM_002241.5(KCNJ10):c.937C>T (p.Pro313Ser)	KCNJ10 (P313S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 205815	NM_002241.5(KCNJ10):c.735C>G (p.Asp245Glu)	KCNJ10 (D245E)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 205827	NM_002241.5(KCNJ10):c.301C>A (p.Pro101Thr)	KCNJ10 (P101T)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance

ClinVar