List of variants in gene combination ATM, C11orf65 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7788+8G>T	rs112775908	0.00166
NM_000051.4(ATM):c.6988C>G (p.Leu2330Val)	rs148432863	0.00075
NM_000051.4(ATM):c.8592C>T (p.Tyr2864=)	rs56025670	0.00051
NM_000051.4(ATM):c.7919C>T (p.Thr2640Ile)	rs4988125	0.00011
NM_000051.4(ATM):c.6096-14A>G	rs184029731	0.00007
NM_000051.4(ATM):c.7521C>T (p.Asp2507=)	rs751234924	0.00006
NM_000051.4(ATM):c.8532T>C (p.Ile2844=)	rs730881278	0.00001
NM_000051.4(ATM):c.6347+31dup	rs58978479

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