List of variants in gene combination ATM, C11orf65 reported as benign for Breast and/or 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6095+15T>C	rs3212321	0.01395
NM_000051.4(ATM):c.6572+12G>T	rs3218677	0.01112
NM_000051.4(ATM):c.8419-19A>G	rs12279930	0.00824
NM_000051.4(ATM):c.6995T>C (p.Leu2332Pro)	rs4988111	0.00660
NM_000051.4(ATM):c.6235G>A (p.Val2079Ile)	rs1800060	0.00649
NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	rs145847315	0.00517
NM_000051.4(ATM):c.6919C>T (p.Leu2307Phe)	rs56009889	0.00035

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