List of variants in gene combination ATM, C11orf65 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6807+238G>C	rs609429	0.53261
NM_000051.4(ATM):c.7788+8G>T	rs112775908	0.00165
NM_000051.4(ATM):c.6176C>T (p.Thr2059Ile)	rs144761622	0.00126
NM_000051.4(ATM):c.6067G>A (p.Gly2023Arg)	rs11212587	0.00124
NM_000051.4(ATM):c.6988C>G (p.Leu2330Val)	rs148432863	0.00075
NM_000051.4(ATM):c.6543G>T (p.Glu2181Asp)	rs138828590	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.6108T>C (p.Tyr2036=)	rs3092826	0.00017
NM_000051.4(ATM):c.7187C>G (p.Thr2396Ser)	rs370559102	0.00017
NM_000051.4(ATM):c.6348-8T>C	rs730881292	0.00011
NM_000051.4(ATM):c.8987+3G>A	rs56360226	0.00001
NM_000051.4(ATM):c.6808-72ATT[4]	rs3212322
NM_000051.4(ATM):c.7516-9dup	rs573494809

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