ClinVar Miner

List of variants reported as benign for Myopathy, lactic acidosis, and sideroblastic anemia 2 by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
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.104C>A (p.Ala35Asp) rs149447502
NM_001040436.3(YARS2):c.1356A>G (p.Gln452=) rs148729348
NM_001040436.3(YARS2):c.291C>T (p.Gly97=) rs11539444
NM_001040436.3(YARS2):c.456G>A (p.Ala152=) rs201940521
NM_001040436.3(YARS2):c.572G>T (p.Gly191Val) rs11539445
NM_001040436.3(YARS2):c.870T>C (p.Val290=) rs142067801

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.