List of variants in gene SDHB reported as likely benign for not provided

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: 36

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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.423+260G>A	rs77244636	0.00660
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.424-170T>G	rs148115746	0.00320
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.642+17T>C	rs200597595	0.00016
NM_003000.3(SDHB):c.113G>A (p.Arg38His)	rs143058777	0.00010
NM_003000.3(SDHB):c.423C>T (p.Pro141=)	rs150542357	0.00009
NM_003000.3(SDHB):c.543C>T (p.Asp181=)	rs199809975	0.00009
NM_003000.3(SDHB):c.200+7A>G	rs371329778	0.00005
NM_003000.3(SDHB):c.606C>T (p.Asn202=)	rs199653121	0.00005
NM_003000.3(SDHB):c.552C>T (p.Tyr184=)	rs202098600	0.00004
NM_003000.3(SDHB):c.73-11A>C	rs927103985	0.00002
NM_003000.3(SDHB):c.287-4T>C	rs200419171	0.00001
NM_003000.3(SDHB):c.33C>T (p.Arg11=)	rs146399542	0.00001
NM_003000.3(SDHB):c.541-9C>T	rs755367242	0.00001
NM_003000.3(SDHB):c.696C>T (p.Ala232=)	rs779143585	0.00001
NM_003000.3(SDHB):c.700C>T (p.Leu234=)	rs201728852	0.00001
NM_003000.2(SDHB):c.424-16_424-14dup	rs34261028
NM_003000.3(SDHB):c.15C>A (p.Val5=)	rs1182998682
NM_003000.3(SDHB):c.15C>G (p.Val5=)	rs1182998682
NM_003000.3(SDHB):c.249T>G (p.Val83=)
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
NM_003000.3(SDHB):c.48A>C (p.Thr16=)	rs1570963474
NM_003000.3(SDHB):c.541-10C>T	rs200004039
NM_003000.3(SDHB):c.541-11T>G	rs1014439132
NM_003000.3(SDHB):c.73-29del	rs745905902
NM_003000.3(SDHB):c.834T>C (p.Ala278=)	rs1570942568

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