ClinVar for MedGen (Select 413851) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809683	NM_001194958.2(KCNJ18):c.364C>T (p.Pro122Ser)	KCNJ18 (P122S)	Single nucleotide variant (missense variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	GUncertain significance
Select item 448965	NM_001194958.2(KCNJ18):c.655C>T (p.Arg219Cys)	KCNJ18 (R219C)	Single nucleotide variant (missense variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	GUncertain significance
Select item 207	NM_001194958.2(KCNJ18):c.1097A>G (p.Lys366Arg)	KCNJ18 (K366R)	Single nucleotide variant (missense variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	Grisk factor
Select item 206	NM_001194958.2(KCNJ18):c.614G>A (p.Arg205His)	KCNJ18 (R205H)	Single nucleotide variant (missense variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	Grisk factor
Select item 205	NM_001194958.2(KCNJ18):c.1061C>T (p.Thr354Met)	KCNJ18 (T354M)	Single nucleotide variant (missense variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	Grisk factor
Select item 204	NM_001194958.2(KCNJ18):c.429del (p.Ile144fs)	KCNJ18 (I144fs)	Deletion (frameshift variant)	Thyrotoxic periodic paralysis, susceptibility to, 2	Grisk factor

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