ClinVar Miner

List of variants reported as uncertain significance for Familial dysautonomia by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 117
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003640.5(ELP1):c.3876T>G (p.Thr1292=) rs61749202 0.01463
NM_003640.5(ELP1):c.1230G>A (p.Pro410=) rs41278359 0.00732
NM_003640.5(ELP1):c.*1214C>T rs143906434 0.00555
NM_003640.5(ELP1):c.*902C>T rs139728295 0.00347
NM_003640.5(ELP1):c.923T>C (p.Leu308Pro) rs78135392 0.00236
NM_003640.5(ELP1):c.1886G>A (p.Arg629His) rs148378319 0.00203
NM_003640.5(ELP1):c.3280A>G (p.Arg1094Gly) rs146440397 0.00098
NM_003640.5(ELP1):c.203G>T (p.Ser68Ile) rs143723093 0.00084
NM_003640.5(ELP1):c.3869A>G (p.Asn1290Ser) rs145319352 0.00083
NM_003640.5(ELP1):c.1213C>T (p.Arg405Trp) rs139703788 0.00076
NM_003640.5(ELP1):c.*1494A>G rs543323193 0.00073
NM_003640.5(ELP1):c.3347-15A>G rs200154542 0.00073
NM_003640.5(ELP1):c.*1489G>A rs78224677 0.00061
NM_003640.5(ELP1):c.3213G>C (p.Glu1071Asp) rs140024352 0.00058
NM_003640.5(ELP1):c.948G>A (p.Pro316=) rs148917889 0.00043
NM_003640.5(ELP1):c.*579A>G rs772683091 0.00041
NM_003640.5(ELP1):c.*502C>T rs56305287 0.00039
NM_003640.5(ELP1):c.1911T>C (p.Val637=) rs369645371 0.00038
NM_003640.5(ELP1):c.2436C>T (p.Asp812=) rs113967847 0.00036
NM_003640.5(ELP1):c.-242T>G rs765585828 0.00032
NM_003640.5(ELP1):c.*1412T>A rs117081559 0.00029
NM_017832.2(ABITRAM):c.-149G>A rs1050167142 0.00027
NM_003640.5(ELP1):c.947C>T (p.Pro316Leu) rs374814563 0.00026
NM_003640.5(ELP1):c.1878C>T (p.Asp626=) rs141596257 0.00021
NM_003640.5(ELP1):c.3474C>T (p.Pro1158=) rs146956297 0.00021
NM_003640.5(ELP1):c.208C>T (p.Arg70Cys) rs3737311 0.00014
NM_003640.5(ELP1):c.3222+14C>T rs374787755 0.00013
NM_003640.5(ELP1):c.*1277T>G rs537888003 0.00012
NM_003640.5(ELP1):c.*1281T>C rs189897190 0.00011
NM_003640.5(ELP1):c.*569T>C rs928660237 0.00011
NM_003640.5(ELP1):c.1073G>A (p.Arg358Gln) rs139091484 0.00011
NM_003640.5(ELP1):c.1704A>G (p.Ser568=) rs138192941 0.00011
NM_003640.5(ELP1):c.3917C>T (p.Ser1306Leu) rs780649768 0.00008
NM_003640.5(ELP1):c.*1240T>C rs1040975275 0.00007
NM_003640.5(ELP1):c.2769A>G (p.Thr923=) rs370330097 0.00007
NM_003640.5(ELP1):c.3259G>A (p.Ala1087Thr) rs61749203 0.00006
NM_003640.5(ELP1):c.3785C>T (p.Thr1262Met) rs199723919 0.00006
NM_003640.5(ELP1):c.2799G>A (p.Arg933=) rs367974002 0.00005
NM_003640.5(ELP1):c.649+12T>C rs375554772 0.00005
NM_003640.5(ELP1):c.*1291A>G rs971258024 0.00004
NM_003640.5(ELP1):c.2026G>A (p.Gly676Ser) rs537930129 0.00004
NM_003640.5(ELP1):c.2861-12T>G rs746590157 0.00004
NM_003640.5(ELP1):c.304-5C>T rs370384351 0.00004
NM_003640.5(ELP1):c.606G>T (p.Gly202=) rs768309637 0.00004
NM_003640.4(ELP1):c.-403C>T rs886063352 0.00003
NM_003640.5(ELP1):c.1614G>C (p.Met538Ile) rs749608070 0.00003
NM_003640.5(ELP1):c.2803A>T (p.Thr935Ser) rs145484092 0.00003
NM_003640.5(ELP1):c.3346+6G>C rs774179813 0.00003
NM_003640.5(ELP1):c.3791A>G (p.Gln1264Arg) rs201888676 0.00003
NM_003640.4(ELP1):c.-323C>T rs901684930 0.00002
NM_003640.4(ELP1):c.-343T>G rs568907421 0.00002
NM_003640.5(ELP1):c.*1062G>T rs559551917 0.00002
NM_003640.5(ELP1):c.*1352A>G rs886063344 0.00002
NM_003640.5(ELP1):c.*1566A>G rs1007495788 0.00002
NM_003640.5(ELP1):c.-115A>T rs932890007 0.00002
NM_003640.5(ELP1):c.2210T>C (p.Met737Thr) rs747028759 0.00002
NM_003640.5(ELP1):c.2958+10A>T rs768709875 0.00002
NM_003640.5(ELP1):c.312T>A (p.Cys104Ter) rs1291760879 0.00002
NM_003640.5(ELP1):c.*1054T>C rs577931217 0.00001
NM_003640.5(ELP1):c.*1194C>T rs1827297908 0.00001
NM_003640.5(ELP1):c.*1511T>C rs758269307 0.00001
NM_003640.5(ELP1):c.-156G>A rs886063350 0.00001
NM_003640.5(ELP1):c.-183C>T rs1437319593 0.00001
NM_003640.5(ELP1):c.1084C>T (p.Leu362Phe) rs774132326 0.00001
NM_003640.5(ELP1):c.1792G>A (p.Gly598Arg) rs886063347 0.00001
NM_003640.5(ELP1):c.2008T>C (p.Phe670Leu) rs376699949 0.00001
NM_003640.5(ELP1):c.2370A>G (p.Glu790=) rs772114554 0.00001
NM_003640.5(ELP1):c.2502-13C>T rs138510668 0.00001
NM_003640.5(ELP1):c.2598C>T (p.Pro866=) rs773218149 0.00001
NM_003640.5(ELP1):c.3144C>T (p.Leu1048=) rs764867856 0.00001
NM_003640.5(ELP1):c.322G>A (p.Val108Ile) rs192047457 0.00001
NM_003640.5(ELP1):c.3513T>C (p.Ser1171=) rs199617076 0.00001
NM_003640.5(ELP1):c.3590G>A (p.Arg1197His) rs886063345 0.00001
NM_003640.5(ELP1):c.3688G>C (p.Glu1230Gln) rs764936574 0.00001
NM_003640.5(ELP1):c.3931+14C>G rs555520875 0.00001
NM_003640.5(ELP1):c.717A>C (p.Gly239=) rs1333495798 0.00001
NM_003640.5(ELP1):c.959-8C>T rs766511916 0.00001
NM_003640.4(ELP1):c.-353C>A rs886063351
NM_003640.5(ELP1):c.*103A>G rs1827336019
NM_003640.5(ELP1):c.*1124C>T rs746907451
NM_003640.5(ELP1):c.*1191T>G rs539404183
NM_003640.5(ELP1):c.*1196G>T rs1827297816
NM_003640.5(ELP1):c.*1254C>A rs879924643
NM_003640.5(ELP1):c.*1406A>G rs1827290161
NM_003640.5(ELP1):c.*1428G>T rs1040481870
NM_003640.5(ELP1):c.*1429C>T rs199666995
NM_003640.5(ELP1):c.*344A>G rs555355380
NM_003640.5(ELP1):c.*636T>C rs1827316671
NM_003640.5(ELP1):c.*705C>T rs1827314926
NM_003640.5(ELP1):c.*769T>A rs1827312944
NM_003640.5(ELP1):c.*806A>C rs549486672
NM_003640.5(ELP1):c.*82G>A rs1827337150
NM_003640.5(ELP1):c.*838C>T rs772279169
NM_003640.5(ELP1):c.-155A>T rs117100816
NM_003640.5(ELP1):c.-158C>G rs530824179
NM_003640.5(ELP1):c.-177C>T rs138630440
NM_003640.5(ELP1):c.-179G>C rs528803158
NM_003640.5(ELP1):c.1390A>C (p.Lys464Gln) rs1829093766
NM_003640.5(ELP1):c.1436CTC[1] (p.Pro480del) rs746116617
NM_003640.5(ELP1):c.1482A>C (p.Glu494Asp) rs1829023404
NM_003640.5(ELP1):c.1655C>G (p.Ala552Gly) rs139891858
NM_003640.5(ELP1):c.169T>C (p.Leu57=) rs886063349
NM_003640.5(ELP1):c.1709T>G (p.Val570Gly) rs886063348
NM_003640.5(ELP1):c.1749G>C (p.Trp583Cys) rs1828896752
NM_003640.5(ELP1):c.178G>C (p.Glu60Gln) rs755988042
NM_003640.5(ELP1):c.1957T>C (p.Leu653=) rs542412132
NM_003640.5(ELP1):c.2052T>A (p.His684Gln) rs1321906641
NM_003640.5(ELP1):c.209G>A (p.Arg70His) rs111936933
NM_003640.5(ELP1):c.209G>T (p.Arg70Leu) rs111936933
NM_003640.5(ELP1):c.2506T>A (p.Cys836Ser) rs879253977
NM_003640.5(ELP1):c.2825G>A (p.Arg942Gln) rs149845612
NM_003640.5(ELP1):c.297A>G (p.Thr99=) rs1829937351
NM_003640.5(ELP1):c.3441A>G (p.Gln1147=) rs779796058
NM_003640.5(ELP1):c.3469G>A (p.Val1157Ile) rs886063346
NM_003640.5(ELP1):c.3572+12A>T rs1055164302
NM_003640.5(ELP1):c.626T>C (p.Val209Ala) rs1039834492
NM_017832.2(ABITRAM):c.-147G>C rs1251331564

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.