ClinVar Miner

List of variants reported as likely benign for NDUFB11-related disorders by PreventionGenetics, part of Exact Sciences

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001135998.3(NDUFB11):c.327G>C (p.Leu109=)	rs182601059	0.00001
NM_001135998.3(NDUFB11):c.198G>A (p.Leu66=)
NM_001135998.3(NDUFB11):c.207+9C>T

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