List of variants in gene combination LOC126860783, SETX reported as uncertain significance for cerebellar ataxia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.-123C>A	rs184570956	0.00017
NM_015046.5(SETX):c.-190G>A	rs1055615359
NM_015046.7(SETX):c.-154G>C	rs886063561

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