List of variants reported as uncertain significance for paragangliomas 4 by Myriad Genetics, Inc.

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.112C>T (p.Arg38Cys)	rs202119350	0.00006
NM_003000.3(SDHB):c.709C>T (p.Pro237Ser)	rs186768244	0.00004
NM_003000.3(SDHB):c.352G>A (p.Asp118Asn)	rs200021702	0.00002
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly)	rs74315369

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