List of variants in gene SDHA studied for Leigh syndrome; Mitochondrial complex II deficiency, nuclear type 1; Dilated cardiomyopathy 1GG; Paragangliomas 5

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1919A>G (p.Glu640Gly)	rs372480044	0.00058
NM_004168.4(SDHA):c.955A>C (p.Ile319Leu)	rs377509915	0.00016
NM_004168.4(SDHA):c.991G>A (p.Ala331Thr)	rs200526913	0.00014
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln)	rs199844384	0.00009
NM_004168.4(SDHA):c.155C>T (p.Ser52Phe)	rs377470390	0.00008
NM_004168.4(SDHA):c.1973C>T (p.Pro658Leu)	rs377632619	0.00004
NM_004168.4(SDHA):c.448G>A (p.Val150Met)	rs542980860	0.00004
NM_004168.4(SDHA):c.739A>G (p.Ile247Val)	rs571292356	0.00004
NM_004168.4(SDHA):c.613T>C (p.Tyr205His)	rs61754481	0.00003
NM_004168.4(SDHA):c.445G>A (p.Ala149Thr)	rs575617625	0.00002
NM_004168.4(SDHA):c.1150T>G (p.Ser384Ala)	rs776888362	0.00001
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp)	rs200397144	0.00001
NM_004168.4(SDHA):c.694C>T (p.Arg232Cys)	rs878854635	0.00001
NM_004168.4(SDHA):c.812C>G (p.Thr271Ser)	rs765611464	0.00001
NM_004168.4(SDHA):c.902A>G (p.Tyr301Cys)	rs182055219	0.00001
NM_004168.4(SDHA):c.994C>T (p.Pro332Ser)	rs373509391

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.