ClinVar Miner

Variants with conflicting interpretations "risk factor" and "affects"

Submission 1 (risk factor) minimum review status: Submission 1 (risk factor) method:
Submission 2 (affects) minimum review status: Submission 2 (affects) method:
ClinVar version:

Total variants with conflicting interpretations: 4

HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.*78C>T rs5848 0.41298
NM_016945.3(TAS2R16):c.516T>G (p.Asn172Lys) rs846664 0.08801
NM_002386.4(MC1R):c.478C>T (p.Arg160Trp) rs1805008 0.04851
NM_002386.4(MC1R):c.451C>T (p.Arg151Cys) rs1805007 0.04832

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