List of variants in gene combination IL4I1, NUP62 reported as uncertain significance for synucleinopathy

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_016553.5(NUP62):c.700A>G (p.Thr234Ala)	rs151022752	0.00019
NM_016553.5(NUP62):c.548C>T (p.Thr183Met)	rs756420654	0.00001
NM_016553.5(NUP62):c.296T>C (p.Leu99Ser)

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