"PreventionGenetics, part of Exact Sciences"[submitter] AND "IL6R"[gen - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1164781	NM_000565.4(IL6R):c.51A>G (p.Gly17=)	IL6R, IL6R-AS1	Single nucleotide variant (synonymous variant)	IL6R-related disorder +1 more	GBenign/Likely benign
Select item 1164401	NM_000565.4(IL6R):c.93G>A (p.Ala31=)	IL6R	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1991296	NM_000565.4(IL6R):c.99C>T (p.Gly33=)	IL6R	Single nucleotide variant (synonymous variant)	IL6R-related disorder +1 more	GLikely benign
Select item 3053397	NM_000565.4(IL6R):c.458+7A>G	IL6R	Single nucleotide variant (intron variant)	IL6R-related disorder	GLikely benign
Select item 1615268	NM_000565.4(IL6R):c.471G>A (p.Pro157=)	IL6R	Single nucleotide variant (synonymous variant +1 more)	IL6R-related disorder +1 more	GLikely benign
Select item 1549725	NM_000565.4(IL6R):c.808-8G>A	IL6R	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3041305	NM_000565.4(IL6R):c.949+1318_949+1320dup	IL6R	Duplication (intron variant)	IL6R-related disorder	GLikely benign
Select item 2688363	NM_000565.4(IL6R):c.949+1320dup	IL6R	Duplication (intron variant)	IL6R-related disorder +1 more	GBenign
Select item 1601641	NM_000565.4(IL6R):c.950-8G>A	IL6R	Single nucleotide variant (intron variant)	IL6R-related disorder +1 more	GBenign/Likely benign
Select item 2186265	NM_000565.4(IL6R):c.950-5C>T	IL6R	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 14660	NM_000565.4(IL6R):c.1073A>C (p.Asp358Ala)	IL6R (D358A)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign
Select item 1509193	NM_000565.4(IL6R):c.1184G>A (p.Arg395Gln)	IL6R (G380R +7 more)	Single nucleotide variant (missense variant)	IL6R-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2163861	NM_000565.4(IL6R):c.1305C>T (p.Ser435=)	IL6R	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2887707	NM_000565.4(IL6R):c.1371T>C (p.Tyr457=)	IL6R	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 783948	NM_000565.4(IL6R):c.1392C>T (p.Tyr464=)	IL6R	Single nucleotide variant (synonymous variant +1 more)	IL6R-related disorder +1 more	GBenign/Likely benign