List of variants in gene combination LOC129929541, SDHB reported as likely benign for central nervous system neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.766-20T>C	rs750144449	0.00001
NM_003000.3(SDHB):c.766-9T>G	rs2077946427	0.00001
NM_003000.3(SDHB):c.766-11C>G
NM_003000.3(SDHB):c.766-14T>C
NM_003000.3(SDHB):c.766-18C>G
NM_003000.3(SDHB):c.766-18C>T
NM_003000.3(SDHB):c.766-19del	rs1553176985
NM_003000.3(SDHB):c.766-21_766-19del
NM_003000.3(SDHB):c.766-6T>C	rs1553176984

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