ClinVar Miner

Variants in gene combination CFTR, LOC111674477 with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 4
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HGVS dbSNP
NM_000492.3(CFTR):c.4243-5C>T rs114402068
NM_000492.3(CFTR):c.4272C>T (p.Tyr1424=) rs1800135
NM_000492.4(CFTR):c.4243-35del rs193922527
NM_000492.4(CFTR):c.4389G>A (p.Gln1463=) rs1800136

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