List of variants reported as likely benign for central nervous system neoplasm by Counsyl

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1664-24del	rs534296796	0.00297
NM_004168.4(SDHA):c.146A>G (p.Asp49Gly)	rs80207011	0.00261
NM_004168.4(SDHA):c.313-19G>T	rs185555941	0.00235
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.287-26A>G	rs201397253	0.00040
NM_003001.5(SDHC):c.20+22G>C	rs182261879	0.00032
NM_003001.5(SDHC):c.405+23C>T	rs373731336	0.00026
NM_004168.4(SDHA):c.895+13G>A	rs201461936	0.00025
NM_003000.3(SDHB):c.642+17T>C	rs200597595	0.00016
NM_003001.5(SDHC):c.179+10G>A	rs532455044	0.00006
NM_004168.4(SDHA):c.1432+7G>C	rs760526397	0.00004
NM_004168.4(SDHA):c.456+9C>T	rs200565489	0.00004
NM_004168.4(SDHA):c.513T>C (p.Arg171=)	rs765157205	0.00004
NM_003000.3(SDHB):c.765+13G>A	rs115561881	0.00002
NM_003000.3(SDHB):c.424-14_424-9dup	rs1064794554
NM_004168.4(SDHA):c.1432+20G>C	rs200127852

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