List of variants in gene VPS13B reported as not provided

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.10219G>A (p.Gly3407Arg)	rs6468694	0.11818
NM_152564.5(VPS13B):c.2485G>A (p.Ala829Thr)	rs61753721	0.00820
NM_152564.5(VPS13B):c.1700G>A (p.Gly567Glu)	rs141046414	0.00054
NM_152564.5(VPS13B):c.983A>G (p.His328Arg)	rs181625846	0.00053
NM_152564.5(VPS13B):c.6657+1G>A	rs180177366	0.00010
NM_152564.5(VPS13B):c.1590G>A (p.Met530Ile)	rs200519753	0.00006
NM_152564.5(VPS13B):c.2075G>A (p.Arg692Gln)	rs371500701	0.00006
GRCh37/hg19 8q22.2(chr8:100133404-100133674)x1
NM_152564.5(VPS13B):c.1651+1G>A	rs758266941
NM_152564.5(VPS13B):c.3348_3349del (p.Cys1117fs)	rs180177327
NM_152564.5(VPS13B):c.3397C>T (p.Pro1133Ser)	rs781781537
NM_152564.5(VPS13B):c.7247+2T>C	rs1563908020
NM_152564.5(VPS13B):c.8384T>C (p.Ile2795Thr)	rs120074155
NM_152564.5(VPS13B):c.9185dup (p.Leu3062fs)	rs180177329

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