List of variants in gene ATM reported as likely pathogenic for Breast carcinoma

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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.875C>T (p.Pro292Leu)	rs747727055	0.00001
NM_000051.4(ATM):c.2839-3_2841del	rs2135547107
NM_000051.4(ATM):c.5755C>T (p.Gln1919Ter)	rs2083823146

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