List of variants in gene SDHAF1 reported as uncertain significance for Mitochondrial complex II deficiency, nuclear type 1

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001042631.3(SDHAF1):c.*229C>T	rs144661239	0.00512
NM_001042631.3(SDHAF1):c.*682A>T	rs554739627	0.00041
NM_001042631.3(SDHAF1):c.*329G>C	rs886054355	0.00004
NM_001042631.3(SDHAF1):c.117T>C (p.His39=)	rs754546603	0.00004
NM_001042631.3(SDHAF1):c.*327C>A	rs1252756289	0.00003
NM_001042631.3(SDHAF1):c.-64C>G	rs886054354	0.00001
NM_001042631.3(SDHAF1):c.*248C>T	rs552373950
NM_001042631.3(SDHAF1):c.*323C>G	rs757546678
NM_001042631.3(SDHAF1):c.*66G>A	rs1976659752
NM_001042631.3(SDHAF1):c.3G>A (p.Met1Ile)	rs1976651034

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