ClinVar Miner

Variants in gene SPG11 with conflicting interpretations "affects" and "benign"

Submission 1 (affects) minimum review status:		Submission 1 (affects) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.833A>G (p.Asn278Ser)	rs75309308

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