List of variants in gene SDHD reported as uncertain significance by Section on Medical Neuroendocrinolgy, National Institutes of Health

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.479G>T (p.Ter160Leu)	rs201372601	0.00002
NM_003002.4(SDHD):c.148C>G (p.His50Asp)	rs779249550
NM_003002.4(SDHD):c.239T>G (p.Leu80Arg)	rs1555187010
NM_003002.4(SDHD):c.328GTT[1] (p.Val111del)	rs1555187580
NM_003002.4(SDHD):c.443G>T (p.Gly148Val)	rs1555187633

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