List of variants in gene WDR81 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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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.218del (p.Leu73fs)	rs1485459176	0.00004
NM_001163809.2(WDR81):c.3997C>T (p.Arg1333Ter)	rs138358708	0.00001
NM_001163809.2(WDR81):c.5335C>T (p.Arg1779Ter)	rs762607878	0.00001
NM_001163809.2(WDR81):c.1564C>T (p.Gln522Ter)	rs1057524638
NM_001163809.2(WDR81):c.1666A>T (p.Lys556Ter)
NM_001163809.2(WDR81):c.2836_2839del (p.Phe946fs)	rs1470681435
NM_001163809.2(WDR81):c.3557del (p.Thr1186fs)	rs1064796183

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