ClinVar Miner

List of variants in gene RELN reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005045.4(RELN):c.6962C>T (p.Thr2321Met) rs116065504 0.00064
NM_005045.4(RELN):c.139G>A (p.Glu47Lys) rs139648092 0.00047
NM_005045.4(RELN):c.7114G>A (p.Val2372Met) rs114344654 0.00046
NM_005045.4(RELN):c.877G>A (p.Asp293Asn) rs200289289 0.00033
NM_005045.4(RELN):c.1231C>A (p.Leu411Ile) rs144978163 0.00021
NM_005045.4(RELN):c.5893C>A (p.Pro1965Thr) rs370624724 0.00019
NM_005045.4(RELN):c.2125A>G (p.Met709Val) rs114577182 0.00018
NM_005045.4(RELN):c.2015C>T (p.Pro672Leu) rs201044262 0.00016
NM_005045.4(RELN):c.4893C>G (p.Asp1631Glu) rs201296719 0.00014
NM_005045.4(RELN):c.6925G>A (p.Asp2309Asn) rs138978280 0.00011
NM_005045.4(RELN):c.4495G>C (p.Asp1499His) rs200428576 0.00009
NM_005045.4(RELN):c.4689C>T (p.Asp1563=) rs138694965 0.00009
NM_005045.4(RELN):c.1566G>C (p.Leu522Phe) rs200373269 0.00006
NM_005045.4(RELN):c.5246A>G (p.Asn1749Ser) rs755596079 0.00006
NM_005045.4(RELN):c.3086T>C (p.Ile1029Thr) rs757915171 0.00005
NM_005045.4(RELN):c.3125C>T (p.Ser1042Leu) rs41276145 0.00005
NM_005045.4(RELN):c.6190C>T (p.His2064Tyr) rs767258528 0.00005
NM_005045.4(RELN):c.2084T>A (p.Phe695Tyr) rs750188972 0.00004
NM_005045.4(RELN):c.2095G>A (p.Ala699Thr) rs543233426 0.00004
NM_005045.4(RELN):c.4042G>A (p.Glu1348Lys) rs773149531 0.00004
NM_005045.4(RELN):c.1555G>T (p.Val519Phe) rs560704715 0.00002
NM_005045.4(RELN):c.1948A>T (p.Ile650Phe) rs371652596 0.00002
NM_005045.4(RELN):c.3941G>A (p.Ser1314Asn) rs561294055 0.00002
NM_005045.4(RELN):c.6311G>A (p.Arg2104His) rs750878959 0.00002
NM_005045.4(RELN):c.6736G>A (p.Val2246Met) rs201561165 0.00002
NM_005045.4(RELN):c.1913C>T (p.Pro638Leu) rs114993407 0.00001
NM_005045.4(RELN):c.230C>T (p.Thr77Ile) rs150587706 0.00001
NM_005045.4(RELN):c.2425C>T (p.Leu809Phe) rs1452060313 0.00001
NM_005045.4(RELN):c.293T>C (p.Val98Ala) rs1471699014 0.00001
NM_005045.4(RELN):c.4369A>C (p.Lys1457Gln) rs890007891 0.00001
NM_005045.4(RELN):c.5179C>T (p.Arg1727Trp) rs757649565 0.00001
NM_005045.4(RELN):c.568C>G (p.Pro190Ala) rs1200261994 0.00001
NM_005045.4(RELN):c.5717T>C (p.Ile1906Thr) rs772921952 0.00001
NM_005045.4(RELN):c.1650G>C (p.Arg550Ser) rs2117391616
NM_005045.4(RELN):c.1789C>T (p.His597Tyr) rs779014769
NM_005045.4(RELN):c.2106G>A (p.Met702Ile)
NM_005045.4(RELN):c.2363C>T (p.Pro788Leu) rs1584363765
NM_005045.4(RELN):c.2485C>T (p.Pro829Ser) rs1832419887
NM_005045.4(RELN):c.2699T>G (p.Leu900Arg) rs1832414894
NM_005045.4(RELN):c.3130G>A (p.Asp1044Asn)
NM_005045.4(RELN):c.3368A>G (p.Asp1123Gly)
NM_005045.4(RELN):c.3745A>G (p.Met1249Val) rs148751867
NM_005045.4(RELN):c.3755T>C (p.Met1252Thr)
NM_005045.4(RELN):c.4010G>C (p.Gly1337Ala) rs1289449043
NM_005045.4(RELN):c.4013G>A (p.Cys1338Tyr)
NM_005045.4(RELN):c.4435G>A (p.Asp1479Asn) rs781311212
NM_005045.4(RELN):c.4747+5G>A
NM_005045.4(RELN):c.4789G>C (p.Gly1597Arg)
NM_005045.4(RELN):c.4842A>G (p.Ile1614Met)
NM_005045.4(RELN):c.4931A>C (p.Asn1644Thr)
NM_005045.4(RELN):c.5011G>C (p.Gly1671Arg) rs939943472
NM_005045.4(RELN):c.5038C>A (p.His1680Asn) rs773182967
NM_005045.4(RELN):c.559A>G (p.Thr187Ala)
NM_005045.4(RELN):c.5612A>G (p.Lys1871Arg) rs769949666
NM_005045.4(RELN):c.5656A>G (p.Ile1886Val)
NM_005045.4(RELN):c.5746A>G (p.Thr1916Ala) rs768731886
NM_005045.4(RELN):c.6047A>G (p.Asn2016Ser)
NM_005045.4(RELN):c.6733C>G (p.Pro2245Ala)
NM_005045.4(RELN):c.7942C>T (p.Leu2648=)
NM_005045.4(RELN):c.874G>C (p.Ala292Pro) rs1478514178

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.