List of variants in gene SDHC reported as benign by Illumina Laboratory Services, Illumina

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_003001.4(SDHC):c.*1335A>G	rs3935401	0.11918
NM_003001.4(SDHC):c.1181_1182insA	rs34067216	0.11567
NM_003001.4(SDHC):c.*2052C>G	rs12239492	0.11550
NM_003001.4(SDHC):c.*968A>G	rs4600063	0.11538
NM_003001.5(SDHC):c.*123C>G	rs3813632	0.08037
NM_003001.4(SDHC):c.*1800G>C	rs72714988	0.04987
NM_003001.4(SDHC):c.*1025G>T	rs16832859	0.02202
NM_003001.4(SDHC):c.*2156A>C	rs116668612	0.02172
NM_003001.5(SDHC):c.*247C>G	rs540126021	0.02155
NM_003001.4(SDHC):c.*2111C>T	rs115166758	0.02148
NM_003001.4(SDHC):c.*1379C>T	rs114731359	0.01951
NM_003001.5(SDHC):c.*612C>T	rs16865495	0.01618
NM_003001.4(SDHC):c.*1323G>A	rs72714986	0.01603
NM_003001.5(SDHC):c.-32T>C	rs115782155	0.01342
NM_003001.5(SDHC):c.*624A>G	rs114438179	0.01340
NM_003001.5(SDHC):c.*469G>A	rs148834287	0.01333
NM_003001.4(SDHC):c.*1731G>A	rs115718047	0.01242
NM_003001.5(SDHC):c.*84G>C	rs201210474	0.00703
NM_003001.5(SDHC):c.*685C>T	rs138085670	0.00295
NM_003001.4(SDHC):c.*1378T>C	rs116141910	0.00273
NM_003001.4(SDHC):c.*1190T>A	rs549554302	0.00021
NM_003001.5(SDHC):c.120G>A (p.Arg40=)	rs36097930	0.00020
NM_003001.4(SDHC):c.*1191A>T	rs566186299	0.00014
NM_003001.5(SDHC):c.*599A>G	rs191744054	0.00006
NM_003001.5(SDHC):c.489T>C (p.Ser163=)	rs559747670	0.00002
NM_003001.4(SDHC):c.*1363A>C	rs555774841	0.00001
NM_003001.5(SDHC):c.*385G>A	rs8266
NM_003001.5(SDHC):c.77+13G>C	rs779727693

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