List of variants in gene SCN3A studied for not specified

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006922.4(SCN3A):c.1441C>T (p.Leu481=)	rs16850131	0.21998
NM_006922.4(SCN3A):c.2547A>C (p.Val849=)	rs62174900	0.16330
NM_006922.4(SCN3A):c.4807+7A>G	rs113867009	0.01340
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.2118G>A (p.Val706=)	rs143450450	0.00160
NM_006922.4(SCN3A):c.5952C>T (p.Asp1984=)	rs145197227	0.00156
NM_006922.4(SCN3A):c.1619C>T (p.Ser540Phe)	rs147678484	0.00112
NM_006922.4(SCN3A):c.2304T>C (p.Ile768=)	rs72870766	0.00072
NM_006922.4(SCN3A):c.5658C>T (p.Val1886=)	rs141161490	0.00063
NM_006922.4(SCN3A):c.3515-9G>T	rs370865394	0.00002
NM_006922.4(SCN3A):c.127_129del (p.Asn43del)	rs72471101
NM_006922.4(SCN3A):c.4239+2dup	rs1553518222

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