ClinVar for MedGen (Select 1768360) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 977233	NM_016562.4(TLR7):c.2383G>T (p.Val795Phe)	TLR7 (V795F)	Single nucleotide variant (missense variant)	Immunodeficiency 74, COVID-19-related, X-linked	GPathogenic
Select item 977232	NM_016562.4(TLR7):c.2129_2132del (p.Gln710fs)	TLR7 (Q710fs)	Deletion (frameshift variant)	Immunodeficiency 74, COVID-19-related, X-linked	GPathogenic