ClinVar Miner

List of variants reported as likely benign for Growth delay due to insulin-like growth factor I resistance

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000875.5(IGF1R):c.*3020dup rs397824885 0.21198
NM_000875.5(IGF1R):c.*910C>T rs702497 0.19953
NM_000875.5(IGF1R):c.*6580C>T rs78536914 0.01529
NM_000875.5(IGF1R):c.*626T>C rs34804698 0.01358
NM_000875.5(IGF1R):c.*15A>G rs45561434 0.01302
NM_000875.5(IGF1R):c.1463-5C>A rs36108138 0.01246
NM_000875.5(IGF1R):c.*134C>T rs55945252 0.01175
NM_000875.5(IGF1R):c.*6329G>A rs142414820 0.00852
NM_000875.5(IGF1R):c.2700C>T (p.Asn900=) rs56400113 0.00749
NM_000875.5(IGF1R):c.*6308T>C rs78894779 0.00588
NM_000875.5(IGF1R):c.*2790C>T rs116869031 0.00552
NM_000875.5(IGF1R):c.*1543A>G rs192125453 0.00535
NM_000875.5(IGF1R):c.*4599C>T rs144947320 0.00511
NM_000875.5(IGF1R):c.1950G>T (p.Arg650=) rs56294552 0.00378
NM_000875.5(IGF1R):c.*5326C>T rs148044985 0.00363
NM_000875.5(IGF1R):c.*3192C>T rs549132136 0.00340
NM_000875.5(IGF1R):c.225C>T (p.Phe75=) rs55770488 0.00312
NM_000875.5(IGF1R):c.1310G>A (p.Arg437His) rs34516635 0.00287
NM_000875.5(IGF1R):c.*3250G>A rs147991406 0.00279
NM_000875.5(IGF1R):c.*458G>A rs35109554 0.00275
NM_000875.5(IGF1R):c.2782+17G>A rs186895929 0.00244
NM_000875.5(IGF1R):c.*43G>A rs56403719 0.00227
NM_000875.5(IGF1R):c.*4762G>A rs141930766 0.00175
NM_000875.5(IGF1R):c.2885+15A>G rs56141459 0.00174
NM_000875.5(IGF1R):c.*3072G>A rs115803157 0.00169
NM_000875.5(IGF1R):c.*6770A>T rs3825952 0.00147
NM_000875.5(IGF1R):c.*352G>A rs183939661 0.00116
NM_000875.5(IGF1R):c.*5909G>A rs187072868 0.00113
NM_000875.5(IGF1R):c.3582C>T (p.Asp1194=) rs35362396 0.00098
NM_000875.5(IGF1R):c.2202-16T>G rs187330252 0.00061
NM_000875.5(IGF1R):c.2558C>T (p.Pro853Leu) rs149217017 0.00053
NM_000875.5(IGF1R):c.*5739T>C rs76014895 0.00046
NM_000875.5(IGF1R):c.*1765T>A rs533982384 0.00035
NM_000875.5(IGF1R):c.*4529T>C rs149893400 0.00035
NM_000875.5(IGF1R):c.*5166C>T rs143549253 0.00024
NM_000875.5(IGF1R):c.3723-4G>A rs185740950 0.00017
NM_000875.5(IGF1R):c.4065C>T (p.Asn1355=) rs45453791 0.00015
NM_000875.5(IGF1R):c.*4439G>C rs554640824 0.00011
NM_000875.5(IGF1R):c.*6942C>T rs535420513 0.00011
NM_000875.5(IGF1R):c.*687C>T rs529711304 0.00010
NM_000875.5(IGF1R):c.*4403C>T rs116383914 0.00009
NM_000875.5(IGF1R):c.*4641C>T rs565859125 0.00004
NM_000875.5(IGF1R):c.*2718C>T rs533651741 0.00002
NM_000875.5(IGF1R):c.*1668C>A rs541647710
NM_000875.5(IGF1R):c.*1753AT[7] rs760831806
NM_000875.5(IGF1R):c.*3440G>A rs146062117
NM_000875.5(IGF1R):c.*3471C>T rs115488157
NM_000875.5(IGF1R):c.*3471dup rs3833014
NM_000875.5(IGF1R):c.*3653C>A rs142786518
NM_000875.5(IGF1R):c.*4466G>C rs184311472
NM_000875.5(IGF1R):c.*4521G>A rs560705462
NM_000875.5(IGF1R):c.*5002T>C rs185728238
NM_000875.5(IGF1R):c.*5736_*5739del rs112539877
NM_000875.5(IGF1R):c.*63A>G rs532740682
NM_000875.5(IGF1R):c.*7046_*7050dup rs373668848
NM_000875.5(IGF1R):c.-41_-33del rs544674838

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.