ClinVar Miner

List of variants in gene ETFB reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001985.3(ETFB):c.-58C>T rs111454736 0.02239
NM_001985.3(ETFB):c.376-292T>C rs139913876 0.01264
NM_001985.3(ETFB):c.375+215G>A rs75898079 0.01137
NM_001985.3(ETFB):c.439-136C>G rs115855517 0.00929
NC_000019.10:g.51366573G>A rs191102821 0.00485
NM_001985.3(ETFB):c.57+46T>G rs183857804 0.00206
NM_001985.3(ETFB):c.521G>A (p.Arg174His) rs141917423 0.00130
NM_001985.3(ETFB):c.709G>A (p.Val237Ile) rs149129214 0.00027
NM_001985.3(ETFB):c.278C>T (p.Pro93Leu) rs139519507 0.00026
NM_001985.3(ETFB):c.58-91C>T rs146798901 0.00021
NM_001985.3(ETFB):c.-16T>C rs374376098 0.00005
NM_001985.3(ETFB):c.582G>A (p.Thr194=) rs376679757 0.00005
NM_001985.3(ETFB):c.597+6C>A rs539989327 0.00004
NM_001985.3(ETFB):c.135G>A (p.Ala45=) rs372040033 0.00003
NM_001985.3(ETFB):c.217-4G>T rs149557388 0.00003
NM_001985.3(ETFB):c.702G>A (p.Thr234=) rs769668781 0.00002
NM_001985.3(ETFB):c.597+8C>T rs758639864 0.00001
NM_001985.3(ETFB):c.598-14C>T rs750381743 0.00001
NC_000019.10:g.51366563GA[2] rs199908626
NM_001985.3(ETFB):c.-44C>A rs751253707
NM_001985.3(ETFB):c.471G>A (p.Gly157=) rs765846018
NM_001985.3(ETFB):c.498C>T (p.Ile166=) rs150636733
NM_001985.3(ETFB):c.519G>C (p.Leu173=) rs933129897
NM_001985.3(ETFB):c.57+36C>T rs186691166
NM_001985.3(ETFB):c.597+17C>A rs372586153

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.