List of variants in gene ATM reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.3118A>G (p.Met1040Val)	rs3092857	0.01233
NM_000051.4(ATM):c.2572T>C (p.Phe858Leu)	rs1800056	0.00861
NM_000051.4(ATM):c.146C>G (p.Ser49Cys)	rs1800054	0.00712
NM_000051.4(ATM):c.186-7C>T	rs55674039	0.00568
NM_000051.4(ATM):c.1810C>T (p.Pro604Ser)	rs2227922	0.00431
NM_000051.4(ATM):c.5497-15G>C	rs3092828	0.00363
NM_000051.4(ATM):c.370A>G (p.Ile124Val)	rs148590073	0.00215
NM_000051.4(ATM):c.162T>C (p.Tyr54=)	rs3218690	0.00200
NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	rs1800059	0.00169
NM_000051.4(ATM):c.2608A>G (p.Asn870Asp)	rs61734354	0.00146
NM_000051.4(ATM):c.1066-6T>G	rs201686625	0.00139
NM_000051.4(ATM):c.4473C>T (p.Phe1491=)	rs4988008	0.00125
NM_000051.4(ATM):c.2127T>C (p.Ile709=)	rs56252953	0.00102
NM_000051.4(ATM):c.2289T>A (p.Phe763Leu)	rs34231402	0.00096
NM_000051.4(ATM):c.3925G>A (p.Ala1309Thr)	rs149711770	0.00081
NM_000051.4(ATM):c.334G>A (p.Ala112Thr)	rs146382972	0.00080
NM_000051.4(ATM):c.3517T>C (p.Leu1173=)	rs141460670	0.00079
NM_000051.4(ATM):c.3150T>C (p.Leu1050=)	rs3092859	0.00076
NM_000051.4(ATM):c.1986T>C (p.Phe662=)	rs1800055	0.00046
NM_000051.4(ATM):c.4709T>C (p.Val1570Ala)	rs140856217	0.00046
NM_000051.4(ATM):c.2932T>C (p.Ser978Pro)	rs139552233	0.00034
NM_000051.4(ATM):c.4949A>G (p.Asn1650Ser)	rs55870064	0.00030
NM_000051.4(ATM):c.3014A>G (p.Asn1005Ser)	rs146531614	0.00028
NM_000051.4(ATM):c.4980C>T (p.Asn1660=)	rs144338238	0.00019
NM_000051.4(ATM):c.1703G>T (p.Arg568Ile)	rs200381392	0.00010
NM_000051.4(ATM):c.5005+7_5005+8del	rs587780626	0.00009
NM_000051.4(ATM):c.2466+7A>G	rs55812024	0.00008
NM_000051.4(ATM):c.2879C>A (p.Pro960His)	rs587779828	0.00001
NM_000051.4(ATM):c.2922-8del	rs373881770
NM_000051.4(ATM):c.2922-8dup	rs373881770
NM_000051.4(ATM):c.5556_5557delinsGA (p.Asp1853Asn)	rs2083595502

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