ClinVar Miner

List of variants in gene MAP3K1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005921.2(MAP3K1):c.1284G>A (p.Thr428=) rs832575 0.83950
NM_005921.2(MAP3K1):c.4257+290G>C rs832548 0.78960
NM_005921.2(MAP3K1):c.2087+298A>G rs33322 0.77412
NM_005921.2(MAP3K1):c.4258-112C>G rs832547 0.77407
NM_005921.2(MAP3K1):c.4389+260T>C rs866222 0.77401
NC_000005.10:g.56815260A>C rs11739344 0.77002
NC_000005.10:g.56815165G>T rs13356762 0.74860
NM_005921.2(MAP3K1):c.483-11C>A rs832567 0.65389
NM_005921.2(MAP3K1):c.482+45C>T rs7731700 0.63175
NM_005921.2(MAP3K1):c.2416G>A (p.Asp806Asn) rs702689 0.61396
NM_005921.2(MAP3K1):c.1301+171C>T rs865570 0.49448
NM_005921.2(MAP3K1):c.3820-11A>G rs3736430 0.11208
NM_005921.2(MAP3K1):c.4258-310T>G rs3817119 0.08922
NM_005921.2(MAP3K1):c.2369+49A>G rs895380 0.08917
NM_005921.2(MAP3K1):c.3084A>G (p.Gln1028=) rs3822625 0.07904
NM_005921.2(MAP3K1):c.2088-92C>T rs9687226 0.05925
NM_005921.2(MAP3K1):c.1687-46C>G rs16886448 0.05775
NM_005921.2(MAP3K1):c.1566C>T (p.Thr522=) rs2229882 0.04382
NM_005921.2(MAP3K1):c.4390-327A>G rs16886478 0.03485
NM_005921.2(MAP3K1):c.3982+264A>G rs77723342 0.03482
NM_005921.2(MAP3K1):c.4390-108C>T rs79797611 0.03250
NM_005921.2(MAP3K1):c.2370-28T>C rs114561358 0.01388
NC_000005.10:g.56815030G>C rs6885541
NC_000005.10:g.56815110G>A rs72758040
NC_000005.10:g.56815110G>C rs72758040
NM_005921.2(MAP3K1):c.1965+254G>T rs72644087
NM_005921.2(MAP3K1):c.4257+195C>T rs832549

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.