ClinVar for MedGen (Select 1804329) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1686934	NM_016562.4(TLR7):c.82A>G (p.Arg28Gly)	TLR7	Single nucleotide variant (missense variant)	Systemic lupus erythematosus 17	GPathogenic
Select item 1686932	NM_016562.4(TLR7):c.790T>C (p.Tyr264His)	TLR7	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1330375	NM_016562.4(TLR7):c.1521T>G (p.Phe507Leu)	TLR7 (F507L)	Single nucleotide variant (missense variant)	Systemic lupus erythematosus 17 +1 more	GPathogenic

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