ClinVar Miner

Variants in gene SERPINA1 with conflicting interpretations "other" and "pathogenic"

Submission 1 (other) minimum review status: Submission 1 (other) method:
Submission 2 (pathogenic) minimum review status: Submission 2 (pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_000295.5(SERPINA1):c.221TCT[2] (p.Phe76del) rs775982338
NM_001127701.1(SERPINA1):c.1096G>A (p.Glu366Lys) rs28929474
NM_001127701.1(SERPINA1):c.1178C>T (p.Pro393Leu) rs199422209
NM_001127701.1(SERPINA1):c.194T>C (p.Leu65Pro) rs28931569
NM_001127701.1(SERPINA1):c.863A>T (p.Glu288Val) rs17580

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