ClinVar Miner

List of intergenic variants studied for hereditary spastic paraplegia 31

Included ClinVar conditions (2):

Hereditary spastic paraplegia 31
Hereditary spastic paraplegia 31; Neuronopathy, distal hereditary motor, type 5B

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NC_000002.11:g.(86479194_86481816)_(86565146_86564634)dup
NC_000002.11:g.(?_86565200)_(86481816_86479194)del

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