List of variants in gene WDR62 reported as likely pathogenic for 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001083961.2(WDR62):c.2520+5G>T	rs754976942	0.00001
NM_001083961.2(WDR62):c.1987AAG[1] (p.Lys664del)	rs764610550
NM_001083961.2(WDR62):c.3361del (p.Ala1121fs)	rs1973468140

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