List of variants in gene WDR81 reported as pathogenic by OMIM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001163809.2(WDR81):c.2567C>T (p.Pro856Leu)	rs587776906	0.00007
NM_001163809.2(WDR81):c.3997C>T (p.Arg1333Ter)	rs138358708	0.00001
NM_001163809.2(WDR81):c.3286C>T (p.Gln1096Ter)	rs770279237
NM_001163809.2(WDR81):c.845G>A (p.Gly282Glu)	rs730882206

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