ClinVar Miner

Variants in gene ATM with conflicting interpretations "uncertain significance" and "risk factor"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (risk factor) minimum review status: Submission 2 (risk factor) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_000051.4(ATM):c.146C>G (p.Ser49Cys) rs1800054 0.00712

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