List of variants in gene KCNQ2 reported 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
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_172107.4(KCNQ2):c.1887+17G>A	rs369457896	0.00091
NM_172107.4(KCNQ2):c.1347C>T (p.Gly449=)	rs771845478	0.00004
NM_172107.4(KCNQ2):c.1888-3C>T	rs772971971	0.00004
NM_172107.4(KCNQ2):c.691-14C>T	rs200448016	0.00004
NM_172107.4(KCNQ2):c.1505C>T (p.Ala502Val)	rs375264483	0.00002
NM_172107.4(KCNQ2):c.1627G>A (p.Val543Met)	rs794727134	0.00001
NM_172107.4(KCNQ2):c.2278C>T (p.Arg760Cys)	rs1449467609	0.00001
NM_172107.4(KCNQ2):c.2300G>A (p.Arg767Gln)	rs752551225	0.00001
NM_172107.4(KCNQ2):c.2555C>T (p.Pro852Leu)	rs745508762	0.00001
NM_172107.4(KCNQ2):c.1687G>A (p.Asp563Asn)	rs796052653
NM_172107.4(KCNQ2):c.173GCGCGGGCG[3] (p.Gly61_Gly63dup)	rs1362316126
NM_172107.4(KCNQ2):c.365C>T (p.Ser122Leu)	rs118192194
NM_172107.4(KCNQ2):c.380A>G (p.Tyr127Cys)	rs796052617
NM_172107.4(KCNQ2):c.620G>A (p.Arg207Gln)	rs118192200
NM_172107.4(KCNQ2):c.638G>A (p.Arg213Gln)
NM_172107.4(KCNQ2):c.917C>T (p.Ala306Val)	rs864321707

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