List of variants in gene combination RELN, SLC26A5 reported as pathogenic for Self-limited epilepsy with centrotemporal spikes

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.8843+3A>C	rs200124755	0.00029
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile)	rs115035120	0.00018
NM_005045.4(RELN):c.9976C>T (p.Arg3326Ter)	rs751409835

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