ClinVar Miner

List of variants in gene combination LOC550113, TMPRSS11F reported as likely benign for not specified

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_207407.2(TMPRSS11F):c.782C>T (p.Ala261Val)	rs1053653951	0.00003
NM_207407.2(TMPRSS11F):c.610C>G (p.Gln204Glu)	rs181704828

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