ClinVar Miner

List of variants reported as benign for neuronopathy, distal hereditary motor, autosomal recessive 8

Included ClinVar conditions (1):

Neuronopathy, distal hereditary motor, autosomal recessive 8

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003104.6(SORD):c.806A>C (p.Asn269Thr)	rs930337	0.23350
NM_003104.6(SORD):c.908+11C>T	rs28495265	0.20727
NM_003104.6(SORD):c.266-35C>T	rs2854446

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