List of variants in gene combination ATM, C11orf65 reported as not provided for not specified

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: 17

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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.6235G>A (p.Val2079Ile)	rs1800060	0.00649
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.6067G>A (p.Gly2023Arg)	rs11212587	0.00124
NM_000051.4(ATM):c.6919C>T (p.Leu2307Phe)	rs56009889	0.00035
NM_000051.4(ATM):c.8734A>G (p.Arg2912Gly)	rs376676328	0.00019
NM_000051.4(ATM):c.7919C>T (p.Thr2640Ile)	rs4988125	0.00011
NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys)	rs531980488	0.00011
NM_000051.4(ATM):c.7988T>C (p.Val2663Ala)	rs377648506	0.00010
NM_000051.4(ATM):c.7757A>G (p.Asn2586Ser)	rs587778079	0.00009
NM_000051.4(ATM):c.8495G>A (p.Arg2832His)	rs529296539	0.00006
NM_000051.4(ATM):c.8545C>T (p.Arg2849Ter)	rs587778080	0.00001
NM_000051.4(ATM):c.8978G>A (p.Arg2993Gln)	rs587778081	0.00001
NM_000051.3(ATM):c.5945A>T (p.Gln1982Leu)	rs543980602
NM_000051.4(ATM):c.5948= (p.Ser1983=)	rs659243
NM_000051.4(ATM):c.6178C>T (p.Arg2060Cys)	rs587778078

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