List of variants in gene UBE2A reported as uncertain significance for X-linked syndromic intellectual disability

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003336.4(UBE2A):c.184G>A (p.Glu62Lys)	rs2053450670
NM_003336.4(UBE2A):c.283C>T (p.Arg95Cys)	rs2053457206
NM_003336.4(UBE2A):c.295A>G (p.Thr99Ala)	rs2053457309
NM_003336.4(UBE2A):c.352C>A (p.Pro118Thr)
NM_003336.4(UBE2A):c.39C>A (p.Phe13Leu)
NM_003336.4(UBE2A):c.403C>T (p.Arg135Trp)	rs767224681

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