ClinVar Miner

Variants with conflicting interpretations "pathogenic" and "confers sensitivity"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (confers sensitivity) minimum review status:		Submission 2 (confers sensitivity) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

HGVS	dbSNP	gnomAD frequency
NM_000511.6(FUT2):c.604C>T (p.Arg202Ter)	rs1800028	0.00057
NM_001130144.3(LTBP3):c.132del (p.Pro45fs)	rs1286042594

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