List of variants in gene RELN reported as likely benign by Illumina Laboratory Services, Illumina

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)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.26A>C (p.Gln9Pro)	rs115165703	0.02037
NM_005045.4(RELN):c.6671+8T>C	rs362758	0.01237
NM_005045.4(RELN):c.6084C>T (p.Gly2028=)	rs114019779	0.00507
NM_005045.4(RELN):c.3712A>C (p.Asn1238His)	rs114003896	0.00468
NM_005045.4(RELN):c.7086C>T (p.Thr2362=)	rs362747	0.00300
NM_005045.4(RELN):c.6228C>T (p.Ser2076=)	rs115379833	0.00291
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met)	rs56342240	0.00287
NM_005045.4(RELN):c.1442-8T>C	rs181761096	0.00212
NM_005045.4(RELN):c.3008+11A>G	rs186983114	0.00174
NM_005045.4(RELN):c.246C>G (p.Thr82=)	rs113242008	0.00171
NM_005045.4(RELN):c.3123C>T (p.Gly1041=)	rs41276148	0.00123
NM_005045.4(RELN):c.3060C>T (p.Asp1020=)	rs115886170	0.00026
NM_005045.4(RELN):c.5088T>C (p.Leu1696=)	rs114551393	0.00016
NM_005045.4(RELN):c.6553A>T (p.Met2185Leu)	rs114686696	0.00010
NM_005045.4(RELN):c.4720G>A (p.Ala1574Thr)	rs78480723	0.00009
NM_005045.4(RELN):c.1555G>T (p.Val519Phe)	rs560704715	0.00002

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