List of variants in gene SCN4A reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.952T>C (p.Trp318Arg)	rs199676994	0.00059
NM_000334.4(SCN4A):c.52C>A (p.Arg18Ser)	rs78592515	0.00054
NM_000334.4(SCN4A):c.367G>A (p.Gly123Arg)	rs377572814	0.00006
NM_000334.4(SCN4A):c.205G>A (p.Gly69Arg)	rs886053249	0.00004
NM_000334.4(SCN4A):c.1378G>A (p.Glu460Lys)	rs540596321	0.00002
NM_000334.4(SCN4A):c.56C>T (p.Pro19Leu)	rs745506979	0.00002
NM_000334.4(SCN4A):c.151G>A (p.Glu51Lys)	rs751390409	0.00001
NM_000334.4(SCN4A):c.307T>G (p.Phe103Val)	rs554349260	0.00001
GRCh37/hg19 17q23.3(chr17:62018758-62067133)x3
NM_000334.4(SCN4A):c.1553G>A (p.Gly518Glu)	rs778649637
NM_000334.4(SCN4A):c.483-5C>T	rs191547933
NM_000334.4(SCN4A):c.644T>C (p.Ile215Thr)	rs1555604867
NM_000334.4(SCN4A):c.716T>A (p.Ile239Asn)	rs1555604652

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