List of variants in gene ATM reported as likely benign by Athena Diagnostics Inc

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.1073A>G (p.Asn358Ser)	rs149636614	0.00079
NM_000051.4(ATM):c.4424A>G (p.Tyr1475Cys)	rs34640941	0.00053
NM_000051.4(ATM):c.4709T>C (p.Val1570Ala)	rs140856217	0.00046
NM_000051.4(ATM):c.4949A>G (p.Asn1650Ser)	rs55870064	0.00030
NM_000051.4(ATM):c.4324T>C (p.Tyr1442His)	rs201666889	0.00029
NM_000051.4(ATM):c.4060C>A (p.Pro1354Thr)	rs145119475	0.00019
NM_000051.4(ATM):c.2522A>C (p.Asp841Ala)	rs587781812	0.00017
NM_000051.4(ATM):c.1773T>C (p.Asn591=)	rs61734356	0.00013
NM_000051.4(ATM):c.1703G>T (p.Arg568Ile)	rs200381392	0.00010
NM_000051.4(ATM):c.5352C>T (p.Asn1784=)	rs140641762	0.00006
NM_000051.4(ATM):c.1368A>G (p.Leu456=)	rs750579940	0.00003
NM_000051.4(ATM):c.2322T>C (p.Gly774=)	rs769575297	0.00001
NM_000051.4(ATM):c.2532A>G (p.Gly844=)	rs755261743	0.00001
NM_000051.4(ATM):c.2934T>G (p.Ser978=)	rs368678134	0.00001
NM_000051.4(ATM):c.3982T>C (p.Leu1328=)	rs876658204	0.00001
NM_000051.4(ATM):c.4731T>A (p.Thr1577=)	rs145236132

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