List of variants in gene SDHA reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.891T>C (p.Pro297=)	rs1126417	0.74998
NM_004168.4(SDHA):c.1932G>A (p.Val644=)	rs6961	0.26598
NM_004168.4(SDHA):c.1038C>G (p.Ser346=)	rs1041949	0.26134
NM_004168.4(SDHA):c.619A>C (p.Arg207=)	rs6555055	0.25190
NM_004168.4(SDHA):c.1752A>G (p.Ala584=)	rs13070	0.25187
NM_004168.4(SDHA):c.684T>C (p.Asn228=)	rs2115272	0.25174
NM_004168.4(SDHA):c.309A>G (p.Ala103=)	rs1139424	0.25161
NM_004168.4(SDHA):c.1680G>A (p.Thr560=)	rs1139449	0.25156
NM_004168.4(SDHA):c.1969G>A (p.Val657Ile)	rs6962	0.18133
NM_004168.4(SDHA):c.1170C>T (p.Phe390=)	rs35277230	0.10356
NM_004168.4(SDHA):c.1664-8G>A	rs199790689	0.01533
NM_004168.4(SDHA):c.1623G>A (p.Lys541=)	rs35502109	0.00206
NM_004168.4(SDHA):c.1368G>A (p.Ser456=)	rs149875171	0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=)	rs144252500	0.00075
NM_004168.4(SDHA):c.723C>T (p.Asp241=)	rs146653693	0.00049
NM_004168.4(SDHA):c.1569T>C (p.Ala523=)	rs150192376	0.00019
NM_004168.4(SDHA):c.1233C>T (p.Gly411=)	rs376530094	0.00003
NM_004168.4(SDHA):c.1974G>C (p.Pro658=)	rs1042446

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.