List of variants in gene KCNT1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_020822.3(KCNT1):c.3312G>A (p.Leu1104=)	rs149416418	0.00671
NM_020822.3(KCNT1):c.3295C>T (p.Pro1099Ser)	rs200642629	0.00491
NM_020822.3(KCNT1):c.3503-18C>T	rs373901872	0.00068
NM_020822.3(KCNT1):c.2619C>T (p.Gly873=)	rs144659358	0.00055
NM_020822.3(KCNT1):c.3681C>T (p.Pro1227=)	rs149049198	0.00034
NM_020822.3(KCNT1):c.3317G>A (p.Arg1106Gln)	rs561255614	0.00014
NM_020822.3(KCNT1):c.1038C>T (p.Phe346=)	rs767434859	0.00002

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