List of variants in gene SDHAF2 reported as likely benign for nervous system cancer

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_017841.4(SDHAF2):c.36+10G>A	rs114207859	0.01460
NM_017841.4(SDHAF2):c.32C>T (p.Ser11Leu)	rs148425779	0.00108
NM_017841.4(SDHAF2):c.6G>A (p.Ala2=)	rs747571875	0.00003
NM_017841.4(SDHAF2):c.269C>T (p.Ala90Val)	rs373951663

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