List of variants in gene RELN reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.4589-8T>G	rs362801	0.01890
NM_005045.4(RELN):c.2932A>G (p.Thr978Ala)	rs3025962	0.01491
NM_005045.4(RELN):c.8086G>A (p.Ala2696Thr)	rs115640958	0.01215
NM_005045.4(RELN):c.6343G>A (p.Gly2115Ser)	rs116716038	0.00747
NM_005045.4(RELN):c.5156C>T (p.Ser1719Leu)	rs115913736	0.00515
NM_005045.4(RELN):c.5108C>G (p.Pro1703Arg)	rs2229860	0.00361
NM_005045.4(RELN):c.5923G>A (p.Gly1975Ser)	rs114807343	0.00300
NM_005045.4(RELN):c.5618C>T (p.Thr1873Ile)	rs41275239	0.00212
NM_005045.4(RELN):c.139G>A (p.Glu47Lys)	rs139648092	0.00047
NM_005045.4(RELN):c.1231C>A (p.Leu411Ile)	rs144978163	0.00021
NM_005045.4(RELN):c.4937-5_4937-4dup	rs35268159

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