List of variants in gene SCN1A reported as likely benign by Illumina Laboratory Services, Illumina

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.345T>C (p.Asn115=)	rs61741123	0.03029
NM_001165963.4(SCN1A):c.1662+9C>A	rs7559148	0.02030
NM_001165963.4(SCN1A):c.1131A>C (p.Arg377=)	rs114137271	0.00322
NM_001165963.4(SCN1A):c.2889T>C (p.Ala963=)	rs144679294	0.00321
NM_001165963.4(SCN1A):c.1811G>A (p.Arg604His)	rs121918769	0.00087
NM_001165963.4(SCN1A):c.2421C>T (p.Phe807=)	rs145101180	0.00062
NM_001165963.4(SCN1A):c.1000C>G (p.Leu334Val)	rs201870762	0.00030
NM_001165963.4(SCN1A):c.1378-3T>C	rs150964803	0.00016
NM_001165963.4(SCN1A):c.1410C>T (p.Ser470=)	rs142571794	0.00015
NM_001165963.4(SCN1A):c.2649C>T (p.Ile883=)	rs543436497	0.00008
NM_001165963.4(SCN1A):c.3012T>C (p.Asp1004=)	rs748537030	0.00002
NM_001165963.4(SCN1A):c.606C>T (p.Tyr202=)	rs374555589	0.00001
NM_001165963.4(SCN1A):c.1171-10_1171-9del	rs372840031
NM_001165963.4(SCN1A):c.2044-5del	rs549232924
NM_001165963.4(SCN1A):c.2177-8dup	rs747086735

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