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

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

Total variants with conflicting interpretations: 4

HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.7190T>C (p.Met2397Thr)	rs3761863	0.61824
NM_000511.6(FUT2):c.461G>A (p.Trp154Ter)	rs601338	0.45281
NM_000511.6(FUT2):c.73A>G (p.Ile25Val)	rs1800021	0.03636
NM_000511.6(FUT2):c.418A>T (p.Ile140Phe)	rs1047781	0.01130

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