ClinVar Miner

List of variants in gene OBSL1 reported as likely benign for Three M syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_015311.3(OBSL1):c.-42T>C rs879691022
NM_015311.3(OBSL1):c.-42del rs757193063
NM_015311.3(OBSL1):c.1102C>T (p.Arg368Cys) rs35009641
NM_015311.3(OBSL1):c.1512C>T (p.Thr504=) rs138262993
NM_015311.3(OBSL1):c.1884C>T (p.Tyr628=) rs115194510
NM_015311.3(OBSL1):c.3816C>T (p.Pro1272=) rs200349173
NM_015311.3(OBSL1):c.4032C>G (p.Pro1344=) rs112751766
NM_015311.3(OBSL1):c.4067-11G>A rs1983211
NM_015311.3(OBSL1):c.4117G>A (p.Glu1373Lys) rs140214067
NM_015311.3(OBSL1):c.4440C>T (p.Ala1480=) rs200341414
NM_015311.3(OBSL1):c.5676G>A (p.Leu1892=) rs3795991
NM_015311.3(OBSL1):c.96G>A (p.Lys32=) rs200451309

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.