List of variants in gene combination LOC121331331, VPS13A reported as uncertain significance for Huntington disease and related disorders

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_033305.3(VPS13A):c.-158G>C	rs1057515644	0.00002
NM_033305.2(VPS13A):c.-183G>A	rs12349389
NM_033305.2(VPS13A):c.-232G>C	rs545092496
NM_033305.2(VPS13A):c.-264G>C	rs542679691

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