List of variants in gene ATM reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.3078-77C>T	rs664677	0.65111
NM_000051.4(ATM):c.2377-56A>G	rs672655	0.48759
NM_000051.4(ATM):c.72+37_72+38del	rs2066734	0.35257
NM_000051.4(ATM):c.5557G>A (p.Asp1853Asn)	rs1801516	0.10783
NM_000051.4(ATM):c.4578C>T (p.Pro1526=)	rs1800889	0.03196
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.4042T>C (p.Leu1348=)	rs56355831	0.00599
NM_000051.4(ATM):c.5005+18G>A	rs76290788	0.00414
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.2442C>A (p.Asp814Glu)	rs3218695
NM_000051.4(ATM):c.3403-13dup	rs3218681
NM_000051.4(ATM):c.497-4dup	rs768748099

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