List of variants in gene SCN3A 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006922.4(SCN3A):c.4432-14T>C	rs73969177	0.00780
NM_006922.4(SCN3A):c.3250G>A (p.Val1084Ile)	rs140990288	0.00518
NM_006922.4(SCN3A):c.171T>C (p.Ala57=)	rs111389453	0.00278
NM_006922.4(SCN3A):c.5232A>G (p.Pro1744=)	rs144587694	0.00035
NM_006922.4(SCN3A):c.2003G>A (p.Gly668Glu)	rs199975643	0.00016
NM_006922.4(SCN3A):c.5200G>C (p.Gly1734Arg)	rs577933870	0.00006
NM_006922.4(SCN3A):c.4186G>A (p.Val1396Met)	rs200031995	0.00005
NM_006922.4(SCN3A):c.2021G>A (p.Gly674Asp)	rs751294193	0.00004
NM_006922.4(SCN3A):c.3253A>G (p.Ile1085Val)	rs144957412	0.00002
NM_006922.4(SCN3A):c.2392-9A>G	rs199781617	0.00001
NM_006922.4(SCN3A):c.137A>C (p.Glu46Ala)	rs1159568725
NM_006922.4(SCN3A):c.603-3_603-2del	rs770371377

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