ClinVar Miner

List of variants in gene combination LOC126860130, RELN, SLC26A5 reported as benign 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.9714C>T (p.His3238=)	rs78218774	0.01139
NM_005045.4(RELN):c.9524A>C (p.His3175Pro)	rs74513461	0.00648

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