List of variants in gene combination ATM, C11orf65 reported as benign by Illumina Laboratory Services, Illumina

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.*3393G>T	rs4585	0.53241
NM_000051.4(ATM):c.*1604C>T	rs227091	0.51797
NM_000051.4(ATM):c.*548G>T	rs227092	0.51711
NM_000051.4(ATM):c.*3072C>T	rs3092844	0.06203
NM_000051.4(ATM):c.*551T>C	rs143531724	0.03007
NM_000051.4(ATM):c.8786+8A>C	rs4986839	0.02488
NM_000051.4(ATM):c.*1427T>C	rs3092836	0.02459
NM_000051.4(ATM):c.*2199C>G	rs75959910	0.02227
NM_000051.4(ATM):c.*2220A>G	rs75293772	0.02223
NM_000051.4(ATM):c.*371A>G	rs3092835	0.01507
NM_000051.4(ATM):c.6095+15T>C	rs3212321	0.01395
NM_000051.4(ATM):c.*3093C>T	rs79807288	0.01336
NM_000051.4(ATM):c.6572+12G>T	rs3218677	0.01112
NM_000051.4(ATM):c.*684T>G	rs3092837	0.01076
NM_000051.4(ATM):c.*1799C>T	rs114847811	0.00725
NM_000051.4(ATM):c.*2080C>T	rs142456486	0.00675
NM_000051.4(ATM):c.6995T>C (p.Leu2332Pro)	rs4988111	0.00660
NM_000051.4(ATM):c.6235G>A (p.Val2079Ile)	rs1800060	0.00649
NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	rs145847315	0.00517
NM_000051.4(ATM):c.*3413T>C	rs4987114	0.00100
NM_000051.4(ATM):c.*540del	rs369583811

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