List of variants in gene SDHAF2 reported as benign by Invitae

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_017841.4(SDHAF2):c.36+10G>A	rs114207859	0.01460
NM_017841.4(SDHAF2):c.36+17T>C	rs201389647	0.00460
NM_017841.4(SDHAF2):c.260+12G>A	rs371469299	0.00108
NM_017841.4(SDHAF2):c.309C>T (p.Asn103=)	rs184314049	0.00050
NM_017841.4(SDHAF2):c.63A>G (p.Leu21=)	rs191513932	0.00025
NM_017841.4(SDHAF2):c.260+25_260+26dup	rs768896122
NM_017841.4(SDHAF2):c.260+26del	rs768896122
NM_017841.4(SDHAF2):c.260+26dup	rs768896122
NM_017841.4(SDHAF2):c.261-19_261-16del

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