ClinVar Miner

List of variants in gene SDHB studied for Inborn genetic diseases

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.115A>G (p.Ile39Val)
NM_003000.3(SDHB):c.299C>T (p.Ser100Phe) rs121917755
NM_003000.3(SDHB):c.625C>T (p.Pro209Ser) rs2101516279

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