List of variants in gene RUSC2 reported as benign for autosomal recessive non-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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014806.5(RUSC2):c.217A>G (p.Thr73Ala)	rs1535422	0.96071
NM_014806.5(RUSC2):c.3342-10C>T	rs2295842	0.17831

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