ClinVar Miner

List of variants in gene combination ATM, C11orf65 reported as uncertain significance by Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7879T>C (p.Tyr2627His)	rs2086422796
NM_000051.4(ATM):c.8948C>T (p.Thr2983Ile)	rs1472935232

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