List of variants reported as likely pathogenic for Paragangliomas 4

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	rs267607032	0.00003
NM_003000.3(SDHB):c.650G>A (p.Arg217His)	rs747518441	0.00003
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln)	rs772551056	0.00001
NM_003000.3(SDHB):c.143A>T (p.Asp48Val)	rs202101384	0.00001
NM_003000.3(SDHB):c.221A>C (p.Asp74Ala)	rs876658713	0.00001
NM_003000.3(SDHB):c.286G>A (p.Gly96Ser)	rs587782243	0.00001
NM_003000.3(SDHB):c.287G>A (p.Gly96Asp)	rs778952116	0.00001
NM_003000.3(SDHB):c.380T>G (p.Ile127Ser)	rs786201095	0.00001
NM_003000.3(SDHB):c.649C>T (p.Arg217Cys)	rs200245469	0.00001
NM_003000.3(SDHB):c.688C>T (p.Arg230Cys)	rs138996609	0.00001
NM_003000.3(SDHB):c.689G>A (p.Arg230His)	rs587782604	0.00001
NM_003000.3(SDHB):c.725G>A (p.Arg242His)	rs74315368	0.00001
NM_003000.3(SDHB):c.137G>T (p.Arg46Leu)	rs772551056
NM_003000.3(SDHB):c.206G>T (p.Gly69Val)	rs2101529108
NM_003000.3(SDHB):c.260T>C (p.Leu87Ser)	rs727504457
NM_003000.3(SDHB):c.277T>C (p.Cys93Arg)	rs727503415
NM_003000.3(SDHB):c.278G>A (p.Cys93Tyr)	rs1131691054
NM_003000.3(SDHB):c.412G>T (p.Asp138Tyr)	rs786203529
NM_003000.3(SDHB):c.424-79_424-2del	rs2525018148
NM_003000.3(SDHB):c.540_540+13del	rs1553177666
NM_003000.3(SDHB):c.565T>C (p.Cys189Arg)	rs2077978513
NM_003000.3(SDHB):c.572G>A (p.Cys191Tyr)	rs2077978456
NM_003000.3(SDHB):c.575G>A (p.Cys192Tyr)	rs397516835
NM_003000.3(SDHB):c.590C>G (p.Pro197Arg)	rs74315367
NM_003000.3(SDHB):c.598dup (p.Trp200fs)	rs2101516417
NM_003000.3(SDHB):c.600G>A (p.Trp200Ter)	rs397516836
NM_003000.3(SDHB):c.640C>T (p.Gln214Ter)	rs876658461
NM_003000.3(SDHB):c.643-1G>A	rs1553177292
NM_003000.3(SDHB):c.72+2T>G	rs1570963414
NM_003000.3(SDHB):c.724C>T (p.Arg242Cys)	rs786203251
NM_003000.3(SDHB):c.765+1G>A	rs2101513511
NM_003000.3(SDHB):c.774_778del (p.Asn258fs)	rs2524995128

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