"GeneDx"[submitter] AND "IL6ST"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1378807	NM_002184.4(IL6ST):c.1000T>C (p.Tyr334His)	IL6ST (Y33H +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1966000	NM_002184.4(IL6ST):c.842G>A (p.Arg281Gln)	IL6ST (R211Q +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 635407	NM_002184.4(IL6ST):c.841C>T (p.Arg281Ter)	IL6ST (R281* +1 more)	Single nucleotide variant (nonsense +2 more)	not provided	GPathogenic

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