ClinVar Miner

List of variants reported as uncertain significance for Duchenne muscular dystrophy by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000109.4(DMD):c.3320T>C (p.Ile1107Thr) rs748123444
NM_004006.2(DMD):c.1687C>T (p.Arg563Cys) rs145739725
NM_004006.2(DMD):c.2330T>C (p.Leu777Pro) rs794727226
NM_004006.2(DMD):c.2912A>T (p.Asp971Val) rs762154042
NM_004006.2(DMD):c.5869C>T (p.Arg1957Trp) rs755477994
NM_004006.2(DMD):c.6409G>C (p.Glu2137Gln) rs1023328955
NM_004006.2(DMD):c.6839G>A (p.Ser2280Asn) rs1060502614
NM_004006.2(DMD):c.9352G>T (p.Ala3118Ser) rs200928985
NM_004006.2(DMD):c.9580A>C (p.Ile3194Leu) rs181517869
NM_004006.3(DMD):c.295A>G (p.Ile99Val) rs149428656

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.