Variants in gene SDHB with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly)	rs11203289	0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.24C>T (p.Ser8=)	rs148738139	0.00461
NM_003000.3(SDHB):c.-37T>C	rs143031690	0.00411
NM_003000.3(SDHB):c.170A>G (p.His57Arg)	rs35962811	0.00231
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.423+20T>A	rs190139590	0.00179
NM_003000.3(SDHB):c.300T>C (p.Ser100=)	rs11541235	0.00157
NM_003000.3(SDHB):c.21C>T (p.Leu7=)	rs147815442	0.00054
NM_003000.3(SDHB):c.158G>A (p.Gly53Glu)	rs34916635	0.00041
NM_003000.3(SDHB):c.552C>T (p.Tyr184=)	rs202098600	0.00004
NM_003000.3(SDHB):c.765+13G>A	rs115561881	0.00002
NM_003000.3(SDHB):c.287-4T>C	rs200419171	0.00001
NM_003000.2(SDHB):c.424-16_424-14dup	rs34261028
NM_003000.3(SDHB):c.424-37TTC[10]	rs34261028
NM_003000.3(SDHB):c.424-37TTC[6]	rs34261028
NM_003000.3(SDHB):c.424-37TTC[7]	rs34261028

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