List of variants in gene SDHD reported as likely benign for Pheochromocytoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_003002.4(SDHD):c.149A>G (p.His50Arg)	rs11214077	0.00679
NM_003002.4(SDHD):c.*622A>G	rs142510105	0.00646
NM_003002.4(SDHD):c.312C>T (p.His104=)	rs61734352	0.00642
NM_003002.4(SDHD):c.*186A>G	rs183918321	0.00328
NM_003002.4(SDHD):c.*352C>G	rs192900956	0.00137

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