C3714580[trait identifier] AND "SIB Swiss Institute of Bioinformatics" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 254842	NM_000069.3(CACNA1S):c.4973G>A (p.Arg1658His)	CACNA1S (R1658H)	Single nucleotide variant (missense variant)	Hypokalemic periodic paralysis, type 1 +4 more	GBenign
Select item 17623	NM_000069.3(CACNA1S):c.3716G>A (p.Arg1239His)	CACNA1S (R1239H)	Single nucleotide variant (missense variant)	Malignant hyperthermia, susceptibility to, 5 +3 more	GConflicting classifications of pathogenicity