List of variants in gene SDHB studied for Mitochondrial complex 2 deficiency, nuclear type 4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.201-36G>T	rs1022580	0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=)	rs2746462	0.95374
NM_003000.3(SDHB):c.113G>A (p.Arg38His)	rs143058777	0.00010
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00003
NM_003000.3(SDHB):c.143A>T (p.Asp48Val)	rs202101384	0.00001
NM_003000.3(SDHB):c.689G>A (p.Arg230His)	rs587782604	0.00001
NM_003000.3(SDHB):c.749C>T (p.Thr250Ile)	rs1057517537	0.00001
NM_003000.3(SDHB):c.769C>G (p.Leu257Val)	rs761350633	0.00001

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