ClinVar Miner

Variants in gene combination HBA1, LOC106804613 with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP
NM_000558.5(HBA1):c.*46C>A rs141514155
NM_000558.5(HBA1):c.-42C>T rs370305736

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