ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as benign for Lissencephaly, Recessive

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP
NM_002474.3(MYH11):c.3700G>A (p.Ala1234Thr) rs16967494
NM_002474.3(MYH11):c.3858+874G>A rs73519694
NM_002474.3(MYH11):c.3859-172T>G rs760024
NM_002474.3(MYH11):c.3859-206C>T rs760023
NM_002474.3(MYH11):c.3859-479C>T rs74009414
NM_002474.3(MYH11):c.3859-558T>C rs16967500
NM_002474.3(MYH11):c.3859-648C>T rs11557090
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=) rs12907
NM_002474.3(MYH11):c.4117-44C>T rs11130
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=) rs1050162
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=) rs1050163
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=) rs28505375

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.