ClinVar Miner

List of variants in gene GFM1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024996.7(GFM1):c.*226C>T rs1047366 0.58206
NM_024996.7(GFM1):c.643G>A (p.Val215Ile) rs2303909 0.58201
NM_024996.7(GFM1):c.18T>C (p.Ala6=) rs1864507 0.58169
NM_024996.7(GFM1):c.998+150G>A rs9858849 0.42309
NM_024996.7(GFM1):c.1324-267G>A rs9878187 0.42275
NM_024996.7(GFM1):c.*6C>T rs1047355 0.42265
NM_024996.7(GFM1):c.1083+82T>C rs9884039 0.42175
NM_024996.7(GFM1):c.81+84C>G rs1864505 0.41996
NM_024996.7(GFM1):c.690-87A>G rs9810874 0.41611
NM_024996.7(GFM1):c.81+22A>G rs1864506 0.36311
NM_024996.7(GFM1):c.1083+57C>T rs62286656 0.36155
NM_024996.7(GFM1):c.368-199G>A rs56075263 0.18998
NM_024996.7(GFM1):c.689+891C>T rs56167308 0.17770
NM_024996.7(GFM1):c.1765-298A>G rs62288305 0.17745
NM_024996.7(GFM1):c.841-224C>T rs55666734 0.17738
NM_024996.7(GFM1):c.-33C>T rs28372852 0.17657
NM_024996.7(GFM1):c.690-96T>A rs56362855 0.17621
NM_024996.5(GFM1):c.-386G>T rs3806642 0.16243
NM_024996.7(GFM1):c.689+611A>G rs73156455 0.15887
NM_024996.7(GFM1):c.1323+83A>G rs2291595 0.15507
NM_024996.7(GFM1):c.367+223C>T rs2303910 0.12733
NM_024996.7(GFM1):c.1323+72A>G rs2291594 0.10832
NM_024996.7(GFM1):c.234+187A>G rs78679143 0.02441
NM_024996.7(GFM1):c.1380+221T>A rs73028945 0.01750
NM_024996.7(GFM1):c.999-221A>T rs78050260 0.01725
NM_024996.7(GFM1):c.-11C>T rs112860155 0.01649
NM_024996.7(GFM1):c.1990G>A (p.Val664Ile) rs62288347 0.01464
NM_024996.7(GFM1):c.476A>G (p.Asn159Ser) rs34297061 0.01238
NM_024996.7(GFM1):c.1601+9G>C rs77186707 0.01234
NM_024996.7(GFM1):c.1083+6T>G rs142919829 0.00940
NM_024996.7(GFM1):c.1209C>T (p.Ala403=) rs149949638 0.00889
NM_024996.7(GFM1):c.127A>G (p.Asn43Asp) rs35942089 0.00886
NM_024996.7(GFM1):c.-31A>G rs28372853 0.00742
NM_024996.7(GFM1):c.2071-17A>G rs76679758 0.00671
NM_024996.7(GFM1):c.568A>C (p.Met190Leu) rs75450876 0.00510
NM_024996.7(GFM1):c.368-18A>G rs185654103 0.00478
NM_024996.7(GFM1):c.1593C>T (p.Ala531=) rs114754676 0.00399
NM_024996.7(GFM1):c.960A>C (p.Pro320=) rs145970222 0.00196
NM_024996.7(GFM1):c.690-5C>G rs201685981 0.00124
NM_024996.7(GFM1):c.2070+11T>G rs150000838 0.00100
NM_024996.7(GFM1):c.235-14G>A rs201304690 0.00053
NM_024996.7(GFM1):c.-38C>T rs377352238 0.00037
NM_024996.7(GFM1):c.77A>G (p.Lys26Arg) rs574200635 0.00002
NM_024996.7(GFM1):c.1519-211T>C rs2115940
NM_024996.7(GFM1):c.1519-25A>G rs7628497
NM_024996.7(GFM1):c.1602-17dup rs11436468
NM_024996.7(GFM1):c.2125-26dup rs145803239
NM_024996.7(GFM1):c.689+1211A>C rs73028908
NM_024996.7(GFM1):c.689+200A>G rs111270770
NM_024996.7(GFM1):c.690-262del rs61079797
NM_024996.7(GFM1):c.81+281_81+283del rs11405116
NM_024996.7(GFM1):c.81+282_81+283del rs11405116
NM_024996.7(GFM1):c.81+283del rs11405116
NM_024996.7(GFM1):c.998+302dup rs11457459

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.