List of variants in gene VPS13D reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015378.4(VPS13D):c.5075G>A (p.Arg1692Gln)	rs201823549	0.00009
NM_015378.4(VPS13D):c.6595A>G (p.Ser2199Gly)	rs545160328	0.00003
NM_015378.4(VPS13D):c.9928G>C (p.Glu3310Gln)	rs756615407	0.00001
NM_015378.4(VPS13D):c.11740G>T (p.Ala3914Ser)

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