List of variants in gene VAPB reported as uncertain significance for Amyotrophic Lateral Sclerosis, Dominant

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)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004738.5(VAPB):c.*5826G>A	rs780911883	0.00025
NM_004738.5(VAPB):c.*6257del	rs750250276	0.00009
NM_004738.5(VAPB):c.5699_5700insA	rs886056830	0.00001
NM_004738.5(VAPB):c.*1451GT[16]	rs138225455
NM_004738.5(VAPB):c.*1451GT[17]	rs138225455
NM_004738.5(VAPB):c.*1451GT[19]	rs138225455
NM_004738.5(VAPB):c.*1451GT[20]	rs138225455
NM_004738.5(VAPB):c.200_214delinsGTTGAGGGGGAAACATTAAAAG	rs386815633
NM_004738.5(VAPB):c.5233_5237del	rs546553846
NM_004738.5(VAPB):c.5511_5513del	rs556955970

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