ClinVar Miner

List of variants reported as benign for Amyotrophic lateral sclerosis type 5; Hereditary spastic paraplegia 11; Charcot-Marie-Tooth disease axonal type 2X by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.6319G>A (p.Val2107Ile)	rs115970214	0.00950
NM_025137.4(SPG11):c.2445-32dup	rs374899647

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