List of variants reported as likely pathogenic for central nervous system neoplasm by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	rs898854295	0.00003
NM_003002.4(SDHD):c.217dup (p.Ser73fs)	rs2135269358
NM_003072.5(SMARCA4):c.3440_3441del (p.Gly1146_Ser1147insTer)
NM_017841.4(SDHAF2):c.42_45del (p.Ala15fs)	rs1862009020

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