List of variants in gene combination ATM, C11orf65 reported as uncertain significance for Familial ovarian cancer

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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)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6096-3T>C	rs748380897	0.00001
NM_000051.4(ATM):c.8987+3G>A	rs56360226	0.00001
NM_000051.4(ATM):c.7466C>A (p.Ser2489Tyr)	rs759728261
NM_000051.4(ATM):c.7927+13dup	rs587781324
NM_000051.4(ATM):c.8597T>C (p.Leu2866Pro)	rs1555139517

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