List of variants in gene combination ATM, C11orf65 reported as likely benign by Counsyl

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	rs145847315	0.00517
NM_000051.4(ATM):c.7788+8G>T	rs112775908	0.00165
NM_000051.4(ATM):c.8010+185_8010+186del	rs984385407	0.00035
NM_000051.4(ATM):c.8584+10T>C	rs373321041	0.00016
NM_000051.4(ATM):c.7494T>C (p.Ser2498=)	rs34393781	0.00010
NM_000051.4(ATM):c.8629T>C (p.Leu2877=)	rs730881279	0.00004
NM_000051.4(ATM):c.6888A>T (p.Ala2296=)	rs200735689	0.00003
NM_000051.4(ATM):c.8100A>G (p.Lys2700=)	rs778601472	0.00003
NM_000051.4(ATM):c.6396A>G (p.Leu2132=)	rs370537345	0.00002
NM_000051.4(ATM):c.7515+20A>G	rs80124497	0.00002
NM_000051.4(ATM):c.6007-10A>G	rs373395916	0.00001
NM_000051.4(ATM):c.7131T>C (p.Asp2377=)	rs373309822	0.00001
NM_000051.4(ATM):c.5918+16A>G	rs3092911
NM_000051.4(ATM):c.7785T>C (p.Asp2595=)	rs34838175
NM_000051.4(ATM):c.8987+10A>G	rs1060504308

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