List of variants in gene TLR7 reported as uncertain significance for autoimmune disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016562.4(TLR7):c.2716G>A (p.Glu906Lys)	rs202022420	0.00003
NM_016562.4(TLR7):c.943A>C (p.Lys315Gln)	rs201359066	0.00001

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