List of variants in gene SDHB reported as pathogenic by OMIM

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00003
NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	rs267607032	0.00003
NM_003000.3(SDHB):c.79C>T (p.Arg27Ter)	rs74315369	0.00003
NM_003000.3(SDHB):c.143A>T (p.Asp48Val)	rs202101384	0.00001
NM_003000.3(SDHB):c.268C>T (p.Arg90Ter)	rs74315366	0.00001
NM_003000.3(SDHB):c.423+1G>A	rs398122805	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.769C>G (p.Leu257Val)	rs761350633	0.00001
NM_003000.3(SDHB):c.(-151_-1)_(72+1_73-1)del
NM_003000.3(SDHB):c.136C>G (p.Arg46Gly)	rs74315370
NM_003000.3(SDHB):c.201-4429_287-934del
NM_003000.3(SDHB):c.299C>T (p.Ser100Phe)	rs121917755
NM_003000.3(SDHB):c.302G>A (p.Cys101Tyr)	rs74315371
NM_003000.3(SDHB):c.395A>C (p.His132Pro)	rs74315372
NM_003000.3(SDHB):c.423+1G>C	rs398122805
NM_003000.3(SDHB):c.590C>G (p.Pro197Arg)	rs74315367
NM_003000.3(SDHB):c.591del (p.Ser198fs)	rs1060503757
NM_003000.3(SDHB):c.716_719del (p.Ser239fs)	rs587781266

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