ClinVar Miner

List of variants in gene NDUFS1 reported as likely pathogenic for MELAS syndrome

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)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.758T>G (p.Val253Gly)	rs786205666

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