List of variants in gene SDHB reported as benign for central nervous system disorder

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.201-36G>T	rs1022580	0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=)	rs2746462	0.95374
NM_003000.3(SDHB):c.642+325C>T	rs2235930	0.51227
NM_003000.3(SDHB):c.200+33G>A	rs2647169	0.10785
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly)	rs11203289	0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.24C>T (p.Ser8=)	rs148738139	0.00461
NM_003000.3(SDHB):c.170A>G (p.His57Arg)	rs35962811	0.00231
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.423+20T>A	rs190139590	0.00179
NM_003000.3(SDHB):c.300T>C (p.Ser100=)	rs11541235	0.00157
NM_003000.3(SDHB):c.21C>T (p.Leu7=)	rs147815442	0.00054
NM_003000.3(SDHB):c.158G>A (p.Gly53Glu)	rs34916635	0.00041
NM_003000.3(SDHB):c.765+13G>A	rs115561881	0.00002
NM_003000.2(SDHB):c.424-16_424-14dup	rs34261028
NM_003000.3(SDHB):c.424-37TTC[10]	rs34261028
NM_003000.3(SDHB):c.424-37TTC[6]	rs34261028
NM_003000.3(SDHB):c.424-37TTC[7]	rs34261028
NM_003000.3(SDHB):c.73-29del	rs745905902
NM_003000.3(SDHB):c.73-7del	rs2101541662

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