List of variants in gene combination ATM, C11orf65 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6995T>C (p.Leu2332Pro)	rs4988111	0.00660
NM_000051.4(ATM):c.5793T>C (p.Ala1931=)	rs3092910	0.00608
NM_000051.4(ATM):c.7788+8G>T	rs112775908	0.00165
NM_000051.4(ATM):c.6067G>A (p.Gly2023Arg)	rs11212587	0.00124
NM_000051.4(ATM):c.7928-10T>C	rs188404773	0.00079
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.6919C>T (p.Leu2307Phe)	rs56009889	0.00035
NM_000051.4(ATM):c.7919C>T (p.Thr2640Ile)	rs4988125	0.00011
NM_000051.4(ATM):c.6888A>T (p.Ala2296=)	rs200735689	0.00003
NM_000051.4(ATM):c.8730C>G (p.Leu2910=)	rs551041839	0.00001
NM_000051.4(ATM):c.8778C>T (p.Val2926=)	rs1430419604

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