List of variants in gene combination LOC126860130, RELN, SLC26A5 reported as uncertain significance for Norman-Roberts syndrome

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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.9708C>T (p.Ser3236=)	rs200370282	0.00008
NM_005045.4(RELN):c.9664A>G (p.Ile3222Val)	rs142638365	0.00001
NM_005045.4(RELN):c.9681T>C (p.Ile3227=)	rs1236487874

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