List of variants reported as benign for Encephalopathy, acute, infection-induced, susceptibility to, 4

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.511C>T (p.Leu171=)	rs2229292	0.02118
NM_000098.3(CPT2):c.1767G>A (p.Thr589=)	rs77565483	0.01032
NM_000098.3(CPT2):c.302C>T (p.Ala101Val)	rs75939866	0.00675
NM_000098.3(CPT2):c.1578T>C (p.Gly526=)	rs113493395	0.00455
NM_000098.3(CPT2):c.588T>C (p.Pro196=)	rs140853350	0.00035
NM_000098.3(CPT2):c.1851T>C (p.His617=)	rs540322467	0.00001

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