ClinVar Miner

List of variants in gene RAD21 reported as uncertain significance for Inborn genetic diseases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006265.3(RAD21):c.1400C>T (p.Ala467Val) rs1445148501 0.00003
NM_006265.3(RAD21):c.1582G>C (p.Glu528Gln) rs750042081 0.00003
NM_006265.3(RAD21):c.1757G>A (p.Arg586Gln) rs780692465 0.00003
NM_006265.3(RAD21):c.1576G>C (p.Glu526Gln) rs373026310 0.00002
NM_006265.3(RAD21):c.1706G>A (p.Arg569His) rs767839436 0.00002
NM_006265.3(RAD21):c.1811A>G (p.Lys604Arg) rs367562161 0.00002
NM_006265.3(RAD21):c.805A>G (p.Asn269Asp) rs376740145 0.00002
NM_006265.3(RAD21):c.1184C>T (p.Pro395Leu) rs149171113 0.00001
NM_006265.3(RAD21):c.1189G>A (p.Val397Ile) rs371948457 0.00001
NM_006265.3(RAD21):c.1276C>T (p.Pro426Ser) rs1033410740 0.00001
NM_006265.3(RAD21):c.1724G>C (p.Gly575Ala) rs762827934 0.00001
NM_006265.3(RAD21):c.539A>C (p.Asp180Ala) rs772085724 0.00001
NM_006265.3(RAD21):c.690T>A (p.Asp230Glu) rs750624995 0.00001
NM_006265.3(RAD21):c.895A>G (p.Asn299Asp) rs760410855 0.00001
NM_006265.3(RAD21):c.1143G>C (p.Trp381Cys) rs2130462808
NM_006265.3(RAD21):c.1228G>A (p.Ala410Thr)
NM_006265.3(RAD21):c.1286A>T (p.Asp429Val) rs763107056
NM_006265.3(RAD21):c.1445A>G (p.Gln482Arg) rs754008925
NM_006265.3(RAD21):c.1453C>G (p.Pro485Ala)
NM_006265.3(RAD21):c.1460C>T (p.Pro487Leu)
NM_006265.3(RAD21):c.160C>T (p.Arg54Trp) rs2130479466
NM_006265.3(RAD21):c.194G>A (p.Arg65Gln) rs773855925
NM_006265.3(RAD21):c.235A>G (p.Asn79Asp) rs1812625374
NM_006265.3(RAD21):c.418G>A (p.Val140Met) rs1554611589
NM_006265.3(RAD21):c.52T>G (p.Trp18Gly) rs2537309018
NM_006265.3(RAD21):c.638A>T (p.Asp213Val) rs1323894024
NM_006265.3(RAD21):c.689A>G (p.Asp230Gly) rs1259261501
NM_006265.3(RAD21):c.703A>G (p.Ser235Gly) rs1812478662
NM_006265.3(RAD21):c.742C>T (p.Leu248Phe)
NM_006265.3(RAD21):c.767C>T (p.Pro256Leu) rs2537296726
NM_006265.3(RAD21):c.790A>G (p.Met264Val)
NM_006265.3(RAD21):c.808G>A (p.Val270Ile)
NM_006265.3(RAD21):c.850G>T (p.Val284Phe) rs760261220
NM_006265.3(RAD21):c.965G>C (p.Arg322Thr) rs2537293003
NM_006265.3(RAD21):c.976G>T (p.Val326Phe) rs1812420919

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.