List of variants in gene combination ATM, C11orf65 reported by True Health Diagnostics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.8786+8A>C	rs4986839	0.02488
NM_000051.4(ATM):c.6995T>C (p.Leu2332Pro)	rs4988111	0.00660
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.7788+8G>T	rs112775908	0.00165
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.5975A>C (p.Lys1992Thr)	rs150757822	0.00025
NM_000051.4(ATM):c.8164C>T (p.Leu2722=)	rs587782399	0.00002
NM_000051.4(ATM):c.8450A>G (p.Tyr2817Cys)	rs747764678	0.00002
NM_000051.4(ATM):c.6974C>T (p.Ala2325Val)	rs200940211	0.00001
NM_000051.4(ATM):c.6975G>C (p.Ala2325=)	rs556778314
NM_000051.4(ATM):c.7012C>G (p.Leu2338Val)	rs1555120990
NM_000051.4(ATM):c.8028A>G (p.Glu2676=)	rs1389648050
NM_000051.4(ATM):c.9008A>G (p.Asn3003Ser)	rs144636562

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