ClinVar Miner

List of variants in gene combination LOC126860131, RELN 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.1336G>C (p.Glu446Gln)	rs56146903	0.00011
NM_005045.4(RELN):c.1344C>G (p.Gly448=)	rs144150588	0.00010

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