List of variants in gene combination ATM, C11orf65 reported as benign for Hereditary cancer-predisposing syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.8851-973A>C	rs170548	0.27178
NM_000051.4(ATM):c.8010+186C>T	rs227060	0.26885
NM_000051.4(ATM):c.8786+8A>C	rs4986839	0.02488
NM_000051.4(ATM):c.6095+15T>C	rs3212321	0.01395
NM_000051.4(ATM):c.6572+12G>T	rs3218677	0.01112
NM_000051.4(ATM):c.8419-19A>G	rs12279930	0.00824
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.5793T>C (p.Ala1931=)	rs3092910	0.00608
NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	rs145847315	0.00517
NM_000051.4(ATM):c.6437G>C (p.Ser2146Thr)	rs56815840	0.00424
NM_000051.4(ATM):c.7630-17T>C	rs116047570	0.00268
NM_000051.4(ATM):c.8269-14A>T	rs114320959	0.00195
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.7313C>T (p.Thr2438Ile)	rs147604227	0.00056
NM_000051.4(ATM):c.7390T>C (p.Cys2464Arg)	rs55801750	0.00038
NM_000051.4(ATM):c.6919C>T (p.Leu2307Phe)	rs56009889	0.00035
NM_000051.4(ATM):c.5975A>C (p.Lys1992Thr)	rs150757822	0.00025
NM_000051.4(ATM):c.6108T>C (p.Tyr2036=)	rs3092826	0.00017
NM_000051.4(ATM):c.9086G>A (p.Gly3029Asp)	rs201199629	0.00016
NM_000051.4(ATM):c.6348-8T>C	rs730881292	0.00011
NM_000051.4(ATM):c.8921C>T (p.Pro2974Leu)	rs139379666	0.00006
NM_000051.4(ATM):c.9006C>T (p.Phe3002=)	rs540172506	0.00003
NM_000051.4(ATM):c.8730C>G (p.Leu2910=)	rs551041839	0.00001
NM_000051.4(ATM):c.5948G>A (p.Ser1983Asn)	rs659243
NM_000051.4(ATM):c.6347+31del	rs58978479
NM_000051.4(ATM):c.7629+13G>A	rs563651647
NM_000051.4(ATM):c.7927+13dup	rs587781324

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