ClinVar Miner

List of variants in gene combination DNM1L, YARS2 reported as likely benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_001040436.3(YARS2):c.*162A>G rs11052215
NM_001040436.3(YARS2):c.*191T>C rs144235100
NM_001040436.3(YARS2):c.*209G>C rs10844337
NM_001040436.3(YARS2):c.*406C>T rs145618550
NM_001040436.3(YARS2):c.*643G>A rs11052214
NM_001040436.3(YARS2):c.1356A>G (p.Gln452=) rs148729348
NM_012062.5(DNM1L):c.*1156G>C rs148183516
NM_012062.5(DNM1L):c.*1213G>T rs11052213
NM_012062.5(DNM1L):c.*1242G>A rs10844336
NM_012062.5(DNM1L):c.*1415T>C rs114366772
NM_012062.5(DNM1L):c.*21G>C rs1059422
NM_012062.5(DNM1L):c.*22A>T rs3200103
NM_012062.5(DNM1L):c.*271C>G rs1020670
NM_012062.5(DNM1L):c.*393A>C rs77298476
NM_012062.5(DNM1L):c.*600C>T rs3600
NM_012062.5(DNM1L):c.*744A>T rs1971911

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.