List of variants in gene combination ATM, C11orf65 reported as uncertain significance by Eurofins NTD LLC (GA)

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.6988C>G (p.Leu2330Val)	rs148432863	0.00075
NM_000051.4(ATM):c.6543G>T (p.Glu2181Asp)	rs138828590	0.00056
NM_000051.4(ATM):c.7313C>T (p.Thr2438Ile)	rs147604227	0.00056
NM_000051.4(ATM):c.6919C>T (p.Leu2307Phe)	rs56009889	0.00035
NM_000051.4(ATM):c.6537T>G (p.Ile2179Met)	rs146243469	0.00022
NM_000051.4(ATM):c.7475T>G (p.Leu2492Arg)	rs56399857	0.00019
NM_000051.4(ATM):c.7187C>G (p.Thr2396Ser)	rs370559102	0.00017
NM_000051.4(ATM):c.8560C>T (p.Arg2854Cys)	rs201958469	0.00013
NM_000051.4(ATM):c.6820G>A (p.Ala2274Thr)	rs567060474	0.00009
NM_000051.4(ATM):c.7757A>G (p.Asn2586Ser)	rs587778079	0.00009
NM_000051.4(ATM):c.6443A>G (p.Lys2148Arg)	rs730881382	0.00006
NM_000051.4(ATM):c.7592T>C (p.Met2531Thr)	rs587781365	0.00004
NM_000051.4(ATM):c.6234C>T (p.Ser2078=)	rs569483748	0.00003
NM_000051.4(ATM):c.6465G>A (p.Val2155=)	rs140423883	0.00003
NM_000051.4(ATM):c.6814G>A (p.Glu2272Lys)	rs886039471	0.00002
NM_000051.4(ATM):c.8987+3G>A	rs56360226	0.00001
NM_000051.4(ATM):c.8518T>C (p.Leu2840=)	rs794727769

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