List of variants in gene VPS13B reported as likely benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.11044+13G>A	rs116819080	0.01028
NM_152564.5(VPS13B):c.9592C>T (p.Arg3198Trp)	rs149842139	0.00511
NM_152564.5(VPS13B):c.11071G>A (p.Ala3691Thr)	rs142476821	0.00312
NM_152564.5(VPS13B):c.7678G>A (p.Glu2560Lys)	rs111751379	0.00304
NM_152564.5(VPS13B):c.11392+8G>A	rs147921058	0.00242
NM_152564.5(VPS13B):c.11195G>A (p.Arg3732Gln)	rs149318176	0.00178
NM_152564.5(VPS13B):c.2651-15A>C	rs370251406	0.00135
NM_152564.5(VPS13B):c.1832G>A (p.Arg611Lys)	rs61754109	0.00116
NM_152564.5(VPS13B):c.10905T>C (p.Pro3635=)	rs61754107	0.00091
NM_152564.5(VPS13B):c.11613C>T (p.Phe3871=)	rs139436386	0.00072
NM_152564.5(VPS13B):c.983A>G (p.His328Arg)	rs181625846	0.00053
NM_152564.5(VPS13B):c.1303-9G>A	rs370251445	0.00006
NM_152564.5(VPS13B):c.5761A>G (p.Thr1921Ala)	rs112749780	0.00003
NM_152564.5(VPS13B):c.581-10T>C	rs770058631	0.00003
NM_152564.5(VPS13B):c.1293T>G (p.Thr431=)	rs77759532

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