Variants in gene SDHB with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.136C>T (p.Arg46Ter)	rs74315370	0.00003
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00001
NM_003000.3(SDHB):c.80G>A (p.Arg27Gln)	rs373976827	0.00001
NM_003000.3(SDHB):c.299C>T (p.Ser100Phe)	rs121917755
NM_003000.3(SDHB):c.642G>C (p.Gln214His)	rs1278834014
Single allele

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