List of variants in gene SDHC reported as benign by GeneDx

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: 39

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.242-174T>C	rs12757174	0.38472
NM_003001.5(SDHC):c.78-283A>C	rs35680024	0.28350
NM_003001.5(SDHC):c.21-96C>T	rs4255403	0.18116
NM_003001.5(SDHC):c.77+32A>T	rs77828459	0.12254
NM_003001.5(SDHC):c.21-211C>T	rs4255402	0.11557
NM_003001.5(SDHC):c.77+186T>C	rs113273303	0.11555
NM_003001.5(SDHC):c.21-189A>G	rs4622080	0.11553
NM_003001.5(SDHC):c.241+74C>T	rs9970904	0.11550
NM_003001.5(SDHC):c.77+519A>G	rs55961103	0.11544
NM_003001.5(SDHC):c.77+428T>G	rs16832826	0.11537
NM_003001.5(SDHC):c.77+344T>C	rs55747162	0.11533
NM_003001.5(SDHC):c.405+299C>G	rs61308286	0.11530
NM_003001.5(SDHC):c.180-313C>T	rs75135629	0.11515
NM_003001.5(SDHC):c.242-136G>T	rs113368293	0.10927
NM_003001.5(SDHC):c.*123C>G	rs3813632	0.08037
NM_003001.5(SDHC):c.78-193T>C	rs60345130	0.07947
NM_003001.5(SDHC):c.77+48C>T	rs112946310	0.07875
NM_003001.5(SDHC):c.20+82T>C	rs11265589	0.07514
NM_003001.5(SDHC):c.241+274C>T	rs11265592	0.05509
NM_003001.5(SDHC):c.77+36T>A	rs117507008	0.04608
NM_003001.5(SDHC):c.20+311C>T	rs60053501	0.02784
NM_003001.5(SDHC):c.180-98G>A	rs115430182	0.02172
NM_003001.5(SDHC):c.*247C>G	rs540126021	0.02155
NM_003001.5(SDHC):c.-32T>C	rs115782155	0.01342
NM_003001.5(SDHC):c.*84G>C	rs201210474	0.00703
NM_003001.5(SDHC):c.180-241_180-240insCTTTG	rs140670104
NM_003001.5(SDHC):c.180-288del	rs78514496
NM_003001.5(SDHC):c.180-289_180-288del	rs78514496
NM_003001.5(SDHC):c.20+11_20+12insTG	rs1571829008
NM_003001.5(SDHC):c.242-154A>C	rs112737166
NM_003001.5(SDHC):c.242-193A>G	rs80246038
NM_003001.5(SDHC):c.405+104dup	rs199612101
NM_003001.5(SDHC):c.405+255_405+256insAATT	rs61234630
NM_003001.5(SDHC):c.405+310C>T	rs61447446
NM_003001.5(SDHC):c.406-14del	rs34744926
NM_003001.5(SDHC):c.77+182C>T	rs111230586
NM_003001.5(SDHC):c.77+248G>A	rs55682614
NM_003001.5(SDHC):c.77+26_77+27insAT	rs202172527
NM_003001.5(SDHC):c.77+28_77+33del	rs2102295921

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