ClinVar Miner

List of variants in gene SDHA reported as likely pathogenic by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.150+1G>A	rs1057523165	0.00001
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp)	rs200397144	0.00001

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