ClinVar Miner

List of variants in gene SPG7 reported as uncertain significance for Spastic Paraplegia, Recessive

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003119.4(SPG7):c.*524dup	rs886052476	0.00001
NM_003119.4(SPG7):c.1780-16_1780-14del	rs863224213

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