List of variants in gene ATM reported as likely benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 22

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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.4578C>T (p.Pro1526=)	rs1800889	0.03196
NM_000051.4(ATM):c.1254A>G (p.Gln418=)	rs4987943	0.02542
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.2119T>C (p.Ser707Pro)	rs4986761	0.00782
NM_000051.4(ATM):c.146C>G (p.Ser49Cys)	rs1800054	0.00712
NM_000051.4(ATM):c.3383A>G (p.Gln1128Arg)	rs2229020	0.00636
NM_000051.4(ATM):c.5558A>T (p.Asp1853Val)	rs1801673	0.00441
NM_000051.4(ATM):c.3993+5G>T	rs3092842	0.00287
NM_000051.4(ATM):c.2362A>C (p.Ser788Arg)	rs641252	0.00265
NM_000051.4(ATM):c.1229T>C (p.Val410Ala)	rs56128736	0.00186
NM_000051.4(ATM):c.4473C>T (p.Phe1491=)	rs4988008	0.00125
NM_000051.4(ATM):c.1986T>C (p.Phe662=)	rs1800055	0.00046
NM_000051.4(ATM):c.3342G>A (p.Lys1114=)	rs138393322	0.00044
NM_000051.4(ATM):c.2346A>G (p.Leu782=)	rs730881285	0.00011
NM_000051.4(ATM):c.5005+7_5005+8del	rs587780626	0.00009
NM_000051.4(ATM):c.4665C>T (p.Leu1555=)	rs374431061	0.00005
NM_000051.4(ATM):c.3219A>G (p.Val1073=)	rs752849892	0.00002
NM_000051.4(ATM):c.5649C>T (p.Ser1883=)	rs1057522721	0.00002
NM_000051.4(ATM):c.3336T>A (p.Pro1112=)	rs758784434	0.00001

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