Variants in gene SDHA with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.146A>G (p.Asp49Gly)	rs80207011	0.00261
NM_004168.4(SDHA):c.1523C>T (p.Thr508Ile)	rs151266052	0.00245
NM_004168.4(SDHA):c.313-19G>T	rs185555941	0.00235
NM_004168.4(SDHA):c.136A>G (p.Lys46Glu)	rs144599870	0.00145
NM_004168.4(SDHA):c.1396G>A (p.Ala466Thr)	rs111387770	0.00097
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_004168.4(SDHA):c.1919A>G (p.Glu640Gly)	rs372480044	0.00058
NM_004168.4(SDHA):c.456+6G>T	rs371735891	0.00047
NM_004168.4(SDHA):c.622-8T>C	rs370714378	0.00037
NM_004168.4(SDHA):c.-2A>T	rs763680697	0.00022
NM_004168.4(SDHA):c.955A>C (p.Ile319Leu)	rs377509915	0.00016
NM_004168.4(SDHA):c.991G>A (p.Ala331Thr)	rs200526913	0.00014
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly)	rs191412461	0.00013
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln)	rs199844384	0.00009
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln)	rs376391115	0.00009
NM_004168.4(SDHA):c.1064+5G>A	rs200021115	0.00006
NM_004168.4(SDHA):c.739A>G (p.Ile247Val)	rs571292356	0.00004
NM_004168.4(SDHA):c.1799G>A (p.Arg600Gln)	rs1126568	0.00002
NM_004168.4(SDHA):c.1242C>T (p.Pro414=)	rs777306884	0.00001
NM_004168.4(SDHA):c.1456C>A (p.Pro486Thr)	rs1060503706	0.00001
NM_004168.4(SDHA):c.92G>A (p.Arg31Gln)	rs752532780	0.00001
NM_004168.4(SDHA):c.-7A>C	rs751633537
NM_004168.4(SDHA):c.1894G>T (p.Val632Phe)	rs369639811
NM_004168.4(SDHA):c.1945_1946del (p.Leu649fs)	rs112307877
NM_004168.4(SDHA):c.830C>T (p.Thr277Met)	rs367721665

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