List of variants in gene VAPB reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004738.5(VAPB):c.*6088C>T	rs147304840	0.00734
NM_004738.5(VAPB):c.*5095T>G	rs143424619	0.00210
NM_004738.5(VAPB):c.510G>A (p.Met170Ile)	rs143144050	0.00170
NM_004738.5(VAPB):c.*5790G>A	rs192046748	0.00126
NM_004738.5(VAPB):c.528G>A (p.Leu176=)	rs199921117	0.00022
NM_004738.5(VAPB):c.476CTT[1] (p.Ser160del)	rs566283411

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