List of variants in gene combination GH-LCR, SCN4A reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.2631T>C (p.Asp877=)	rs79893125	0.08466
NM_000334.4(SCN4A):c.2919C>T (p.Pro973=)	rs73992419	0.03148
NM_000334.4(SCN4A):c.4288+10G>T	rs114059193	0.03137
NM_000334.4(SCN4A):c.2989+5G>A	rs115695396	0.02066
NM_000334.4(SCN4A):c.2289C>T (p.Ile763=)	rs76894284	0.01359
NM_000334.4(SCN4A):c.2717G>C (p.Ser906Thr)	rs41280102	0.01003
NM_000334.4(SCN4A):c.3441+7G>A	rs142270113	0.00738
NM_000334.4(SCN4A):c.4690G>A (p.Val1564Ile)	rs202106192	0.00108
NM_000334.4(SCN4A):c.5274C>T (p.His1758=)	rs113418988	0.00051
NM_000334.4(SCN4A):c.5037C>T (p.Ile1679=)	rs372002602	0.00019
NM_000334.4(SCN4A):c.2328C>T (p.Ala776=)	rs367936207	0.00001
NM_000334.4(SCN4A):c.3604G>A (p.Glu1202Lys)	rs201916531	0.00001

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