List of variants in gene VPS13B reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.2485G>A (p.Ala829Thr)	rs61753721	0.00820
NM_152564.5(VPS13B):c.3203C>T (p.Thr1068Ile)	rs61753722	0.00690
NM_152564.5(VPS13B):c.6977G>A (p.Arg2326Gln)	rs61754113	0.00651
NM_152564.5(VPS13B):c.10049C>T (p.Thr3350Ile)	rs138127778	0.00637
NM_152564.5(VPS13B):c.8903A>G (p.Asn2968Ser)	rs28940272	0.00396
NM_152564.5(VPS13B):c.7678G>A (p.Glu2560Lys)	rs111751379	0.00304
NM_152564.5(VPS13B):c.10235C>T (p.Ala3412Val)	rs112045467	0.00251
NM_152564.5(VPS13B):c.2596G>A (p.Val866Ile)	rs150185067	0.00076
NM_152564.5(VPS13B):c.1559A>G (p.His520Arg)	rs143205296	0.00068
NM_152564.5(VPS13B):c.2377C>G (p.Leu793Val)	rs141638933	0.00020
NM_152564.5(VPS13B):c.8429A>C (p.Gln2810Pro)	rs769551176	0.00001
NM_152564.5(VPS13B):c.6857A>G (p.Gln2286Arg)	rs200713917

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