ClinVar Miner

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

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.1377G>A (p.Arg459=)	rs73712207	0.00185
NM_005045.4(RELN):c.1386C>T (p.Cys462=)	rs139321058	0.00046

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