List of variants in gene 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)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
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.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.1596G>A (p.Gln532=)	rs41276154	0.04078
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.26A>C (p.Gln9Pro)	rs115165703	0.02037
NM_005045.4(RELN):c.7110T>C (p.Val2370=)	rs362746	0.01926
NM_005045.4(RELN):c.2932A>G (p.Thr978Ala)	rs3025962	0.01491
NM_005045.4(RELN):c.6671+8T>C	rs362758	0.01237
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.5156C>T (p.Ser1719Leu)	rs115913736	0.00515
NM_005045.4(RELN):c.7086C>T (p.Thr2362=)	rs362747	0.00300
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met)	rs56342240	0.00287
NM_005045.4(RELN):c.906C>T (p.Ala302=)	rs114494558	0.00287
NM_005045.4(RELN):c.416C>G (p.Thr139Ser)	rs79471015	0.00283
NM_005045.4(RELN):c.4408G>A (p.Val1470Ile)	rs143213152	0.00232
NM_005045.4(RELN):c.246C>G (p.Thr82=)	rs113242008	0.00171
NM_005045.4(RELN):c.3477C>A (p.Asn1159Lys)	rs114684479	0.00140
NM_005045.4(RELN):c.6141C>T (p.Phe2047=)	rs79161241	0.00098
NM_005045.4(RELN):c.3663C>T (p.Ser1221=)	rs199705497	0.00019
NM_005045.4(RELN):c.2532G>A (p.Pro844=)	rs113842330	0.00016
NM_005045.4(RELN):c.5599A>C (p.Arg1867=)	rs753376558	0.00004
NM_005045.4(RELN):c.6888G>A (p.Pro2296=)	rs142792443	0.00003
NM_005045.4(RELN):c.5832C>T (p.Phe1944=)	rs767598814	0.00002
NM_005045.4(RELN):c.2442A>G (p.Ser814=)	rs759128344	0.00001
NM_005045.4(RELN):c.6771G>A (p.Ser2257=)	rs367867782	0.00001

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