List of variants in gene SDHC reported as likely benign for not provided

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.78-152C>T	rs140984949	0.00649
NM_003001.5(SDHC):c.242-176T>C	rs188698798	0.00370
NM_003001.5(SDHC):c.*78G>A	rs182629842	0.00182
NM_003001.5(SDHC):c.180-135G>A	rs187490191	0.00146
NM_003001.5(SDHC):c.405+23C>T	rs373731336	0.00026
NM_003001.5(SDHC):c.78-19C>T	rs144770080	0.00023
NM_003001.5(SDHC):c.120G>A (p.Arg40=)	rs36097930	0.00020
NM_003001.5(SDHC):c.342C>T (p.His114=)	rs143730978	0.00019
NM_003001.5(SDHC):c.405+13G>A	rs369274171	0.00008
NM_003001.5(SDHC):c.444A>C (p.Leu148=)	rs377230417	0.00004
NM_003001.5(SDHC):c.490A>T (p.Met164Leu)	rs200375156	0.00004
NM_003001.5(SDHC):c.99G>A (p.Thr33=)	rs145535502	0.00003
NM_003001.5(SDHC):c.489T>C (p.Ser163=)	rs559747670	0.00002
NM_003001.5(SDHC):c.9G>A (p.Ala3=)	rs749265569	0.00001
NM_003001.5(SDHC):c.12G>T (p.Leu4=)	rs745443094
NM_003001.5(SDHC):c.21-10dup	rs759481419
NM_003001.5(SDHC):c.24C>T (p.His8=)	rs761381438
NM_003001.5(SDHC):c.294T>G (p.Ser98=)	rs376292127
NM_003001.5(SDHC):c.406-14dup	rs34744926
NM_003001.5(SDHC):c.77+29_77+31dup	rs371604278
NM_003001.5(SDHC):c.78-19C>A	rs144770080

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