List of variants in gene VPS13B reported as benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.1206+33T>G	rs7460625	0.73774
NM_152564.5(VPS13B):c.10061+24G>A	rs34513504	0.23936
NM_152564.5(VPS13B):c.9492T>C (p.Ser3164=)	rs36074608	0.15932
NM_152564.5(VPS13B):c.10219G>A (p.Gly3407Arg)	rs6468694	0.11916
NM_152564.5(VPS13B):c.7676T>C (p.Val2559Ala)	rs7833870	0.09284
NM_152564.5(VPS13B):c.6963A>G (p.Val2321=)	rs61753724	0.07191
NM_152564.5(VPS13B):c.3667-7C>T	rs35543295	0.03607
NM_152564.5(VPS13B):c.10065G>T (p.Ala3355=)	rs61753726	0.01526
NM_152564.5(VPS13B):c.9330+10T>A	rs75904081	0.01493
NM_152564.5(VPS13B):c.11044+13G>A	rs116819080	0.01028
NM_152564.5(VPS13B):c.2934+14A>T	rs187151724	0.00690
NM_152564.5(VPS13B):c.8570C>T (p.Pro2857Leu)	rs145890213	0.00068
NM_152564.5(VPS13B):c.8171A>G (p.Tyr2724Cys)	rs138453594	0.00001
NM_152564.5(VPS13B):c.1293T>G (p.Thr431=)	rs77759532

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