ClinVar Miner

List of variants in gene SRP72 reported as benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
NM_006947.4(SRP72):c.*1313C>G rs113719942
NM_006947.4(SRP72):c.*139G>A rs28438730
NM_006947.4(SRP72):c.*1603A>G rs1142851
NM_006947.4(SRP72):c.*173T>C rs10051
NM_006947.4(SRP72):c.*386G>A rs4260596
NM_006947.4(SRP72):c.*442A>G rs7762
NM_006947.4(SRP72):c.*622_*649del rs59791697
NM_006947.4(SRP72):c.*732A>G rs14211
NM_006947.4(SRP72):c.*780C>T rs10518
NM_006947.4(SRP72):c.1410A>G (p.Leu470=) rs17086879
NM_006947.4(SRP72):c.1671A>G (p.Lys557=) rs34419325
NM_006947.4(SRP72):c.19G>T (p.Gly7Trp) rs17524437
NM_006947.4(SRP72):c.21G>T (p.Gly7=) rs12513091
NM_006947.4(SRP72):c.686A>G (p.His229Arg) rs138986942

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.