List of variants in gene DHODH reported as benign for bone development disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001361.5(DHODH):c.435-38G>C	rs11075914	0.99994
NM_001361.5(DHODH):c.*1051A>G	rs2287999	0.55850
NM_001361.5(DHODH):c.*783A>G	rs2288000	0.55819
NM_001361.5(DHODH):c.*1171T>C	rs2287998	0.55799
NM_001361.5(DHODH):c.*574G>T	rs2288001	0.55770
NM_001361.5(DHODH):c.518-39G>T	rs1862752	0.54545
NM_001361.5(DHODH):c.19A>C (p.Lys7Gln)	rs3213422	0.54012
NM_001361.5(DHODH):c.*569G>A	rs113365769	0.10579
NM_001361.5(DHODH):c.*595C>T	rs111810095	0.04483
NM_001361.5(DHODH):c.*612T>C	rs7191724	0.04342
NM_001361.5(DHODH):c.819+10G>A	rs114267707	0.01597
NM_001361.5(DHODH):c.*1014C>T	rs79926352	0.01533
NM_001361.5(DHODH):c.*748C>T	rs117655998	0.01294
NM_001361.5(DHODH):c.573G>A (p.Ala191=)	rs148523165	0.00894
NM_001361.5(DHODH):c.457C>A (p.Leu153Ile)	rs61741731	0.00410

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.