List of variants in gene RELN reported as benign for Norman-Roberts syndrome

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.7181-34G>A	rs362706	0.75362
NM_005045.4(RELN):c.8046T>C (p.His2682=)	rs2229864	0.49951
NM_005045.4(RELN):c.578-3T>C	rs607755	0.49658
NM_005045.4(RELN):c.4589-28A>G	rs362726	0.46847
NM_005045.4(RELN):c.7887T>C (p.Pro2629=)	rs56345626	0.17070
NM_005045.4(RELN):c.2989C>G (p.Leu997Val)	rs362691	0.10133
NM_005045.4(RELN):c.1776A>G (p.Glu592=)	rs2072403	0.09661
NM_005045.4(RELN):c.6702T>C (p.Cys2234=)	rs2075043	0.05938
NM_005045.4(RELN):c.4588+14T>C	rs362810	0.04203
NM_005045.4(RELN):c.1596G>A (p.Gln532=)	rs41276154	0.04078
NM_005045.4(RELN):c.7530C>T (p.Pro2510=)	rs2075038	0.03404
NM_005045.4(RELN):c.5351+3A>G	rs6967725	0.03307
NM_005045.4(RELN):c.5831T>G (p.Phe1944Cys)	rs77664442	0.02460
NM_005045.4(RELN):c.6672-15G>A	rs73418565	0.02349
NM_005045.4(RELN):c.1888A>C (p.Ser630Arg)	rs115734214	0.02229
NM_005045.4(RELN):c.7110T>C (p.Val2370=)	rs362746	0.01926
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.3839G>A (p.Gly1280Glu)	rs55689103	0.01176
NM_005045.4(RELN):c.1799C>T (p.Ser600Phe)	rs78008536	0.01065
NM_005045.4(RELN):c.5284G>A (p.Val1762Ile)	rs79499902	0.01040
NM_005045.4(RELN):c.6343G>A (p.Gly2115Ser)	rs116716038	0.00747
NM_005045.4(RELN):c.6078C>T (p.Asn2026=)	rs79610081	0.00676
NM_005045.4(RELN):c.621C>T (p.Asp207=)	rs114627891	0.00558
NM_005045.4(RELN):c.1075G>A (p.Val359Ile)	rs114926265	0.00535
NM_005045.4(RELN):c.5156C>T (p.Ser1719Leu)	rs115913736	0.00515
NM_005045.4(RELN):c.4937-15A>T	rs2711839	0.00514
NM_005045.4(RELN):c.1824C>T (p.Cys608=)	rs79620906	0.00502
NM_005045.4(RELN):c.5775A>G (p.Arg1925=)	rs2711866	0.00464
NM_005045.4(RELN):c.7538C>G (p.Ser2513Cys)	rs114647348	0.00354
NM_005045.4(RELN):c.5923G>A (p.Gly1975Ser)	rs114807343	0.00300
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met)	rs56342240	0.00287
NM_005045.4(RELN):c.416C>G (p.Thr139Ser)	rs79471015	0.00283
NM_005045.4(RELN):c.5618C>T (p.Thr1873Ile)	rs41275239	0.00212
NM_005045.4(RELN):c.3477C>A (p.Asn1159Lys)	rs114684479	0.00140
NM_005045.4(RELN):c.4748-11T>C	rs201494847	0.00098
NM_005045.4(RELN):c.7111G>A (p.Ala2371Thr)	rs79377093	0.00084
NM_005045.4(RELN):c.1144-15T>C	rs2301560	0.00025
NM_005045.4(RELN):c.-24GGC[10] (p.Met1_Glu2insGlyGly)	rs55656324
NM_005045.4(RELN):c.4937-4del	rs35268159
NM_005045.4(RELN):c.6303-42_6303-40del	rs74440147

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