List of variants reported as likely benign for Paragangliomas 5

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Total variants: 24

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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_004168.4(SDHA):c.1368G>A (p.Ser456=)	rs149875171	0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=)	rs144252500	0.00075
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_004168.4(SDHA):c.456+6G>T	rs371735891	0.00047
NM_004168.4(SDHA):c.622-8T>C	rs370714378	0.00037
NM_004168.4(SDHA):c.895+13G>A	rs201461936	0.00025
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly)	rs191412461	0.00013
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln)	rs199844384	0.00009
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln)	rs376391115	0.00009
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_004168.4(SDHA):c.1737C>T (p.Ile579=)	rs201454617	0.00002
NM_004168.4(SDHA):c.1182C>T (p.Asp394=)	rs377317558	0.00001
NM_004168.4(SDHA):c.1308C>T (p.Tyr436=)	rs762494024	0.00001
NM_004168.4(SDHA):c.1323C>T (p.Ala441=)	rs751561561	0.00001
NM_004168.4(SDHA):c.1410C>T (p.Ser470=)	rs556476038	0.00001
NM_004168.4(SDHA):c.896-4G>A	rs555881974	0.00001
NM_004168.4(SDHA):c.-7A>C	rs751633537
NM_004168.4(SDHA):c.1432+20G>C	rs200127852
NM_004168.4(SDHA):c.830C>T (p.Thr277Met)	rs367721665

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