List of variants in gene combination ATM, C11orf65 reported as benign by Sema4, Sema4

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: 11

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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.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.6108T>C (p.Tyr2036=)	rs3092826	0.00017
NM_000051.4(ATM):c.6348-8T>C	rs730881292	0.00011
NM_000051.4(ATM):c.9006C>T (p.Phe3002=)	rs540172506	0.00003
NM_000051.4(ATM):c.8730C>G (p.Leu2910=)	rs551041839	0.00001

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