List of variants in gene VPS13B reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.9492T>C (p.Ser3164=)	rs36074608	0.16279
NM_152564.5(VPS13B):c.6963A>G (p.Val2321=)	rs61753724	0.06924
NM_152564.5(VPS13B):c.10065G>T (p.Ala3355=)	rs61753726	0.01526
NM_152564.5(VPS13B):c.2934+14A>T	rs187151724	0.00690
NM_152564.5(VPS13B):c.3203C>T (p.Thr1068Ile)	rs61753722	0.00690
NM_152564.5(VPS13B):c.2451T>C (p.His817=)	rs114120664	0.00630
NM_152564.5(VPS13B):c.9592C>T (p.Arg3198Trp)	rs149842139	0.00511
NM_152564.5(VPS13B):c.3386A>G (p.Lys1129Arg)	rs61759485	0.00445
NM_152564.5(VPS13B):c.7678G>A (p.Glu2560Lys)	rs111751379	0.00304
NM_152564.5(VPS13B):c.8171A>G (p.Tyr2724Cys)	rs138453594	0.00050
NM_152564.5(VPS13B):c.6455-4dup	rs398124337

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