List of variants in gene ATM reported as benign for Breast and/or ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.378T>A (p.Asp126Glu)	rs2234997	0.06244
NM_000051.4(ATM):c.3403-15T>A	rs79701258	0.02975
NM_000051.4(ATM):c.657T>C (p.Cys219=)	rs2235003	0.02841
NM_000051.4(ATM):c.1254A>G (p.Gln418=)	rs4987943	0.02542
NM_000051.4(ATM):c.2639-17G>T	rs2234994	0.02161
NM_000051.4(ATM):c.4138C>T (p.His1380Tyr)	rs3092856	0.02156
NM_000051.4(ATM):c.1541G>A (p.Gly514Asp)	rs2235000	0.01889
NM_000051.4(ATM):c.186-17A>G	rs4987907	0.01587
NM_000051.4(ATM):c.2193C>T (p.Tyr731=)	rs2229019	0.01543
NM_000051.4(ATM):c.1636C>G (p.Leu546Val)	rs2227924	0.01541
NM_000051.4(ATM):c.2614C>T (p.Pro872Ser)	rs3218673	0.01393
NM_000051.4(ATM):c.2685A>G (p.Leu895=)	rs3218687	0.01393
NM_000051.4(ATM):c.3118A>G (p.Met1040Val)	rs3092857	0.01233
NM_000051.4(ATM):c.4258C>T (p.Leu1420Phe)	rs1800058	0.01150
NM_000051.4(ATM):c.2572T>C (p.Phe858Leu)	rs1800056	0.00861
NM_000051.4(ATM):c.4042T>C (p.Leu1348=)	rs56355831	0.00599
NM_000051.4(ATM):c.186-7C>T	rs55674039	0.00568
NM_000051.4(ATM):c.5558A>T (p.Asp1853Val)	rs1801673	0.00441
NM_000051.4(ATM):c.1810C>T (p.Pro604Ser)	rs2227922	0.00431
NM_000051.4(ATM):c.1176C>G (p.Gly392=)	rs1800727	0.00388
NM_000051.4(ATM):c.5497-15G>C	rs3092828	0.00363
NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	rs1800059	0.00169
NM_000051.4(ATM):c.2127T>C (p.Ile709=)	rs56252953	0.00102
NM_000051.4(ATM):c.1236-3del	rs34325032
NM_000051.4(ATM):c.1236-3dup	rs34325032
NM_000051.4(ATM):c.1236-4_1236-3del	rs34325032
NM_000051.4(ATM):c.2442C>A (p.Asp814Glu)	rs3218695
NM_000051.4(ATM):c.2922-8del	rs373881770
NM_000051.4(ATM):c.2922-9_2922-8del
NM_000051.4(ATM):c.3403-13dup	rs3218681
NM_000051.4(ATM):c.3403-15dup	rs1555091083

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