ClinVar Miner

List of variants in gene MAP3K20 reported as benign for Split-foot malformation-mesoaxial polydactyly syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016653.3(MAP3K20):c.670-11G>C rs11899707 0.98158
NM_016653.3(MAP3K20):c.1360-28A>G rs820008 0.72578
NM_016653.3(MAP3K20):c.445-37A>G rs2289399 0.30550
NM_016653.3(MAP3K20):c.1032+39G>A rs16861404 0.26026
NM_016653.3(MAP3K20):c.1592C>T (p.Ser531Leu) rs3769148

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.