List of variants in gene WDR35 reported as likely pathogenic for autosomal recessive disease

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.1889T>G (p.Leu630Ter)	rs199952377	0.00019
NM_020779.4(WDR35):c.2415-2A>G	rs143550695	0.00005
NM_020779.4(WDR35):c.1255+1G>A	rs371669862	0.00004
NM_020779.4(WDR35):c.932G>T (p.Trp311Leu)	rs200649783	0.00003
NM_020779.4(WDR35):c.1382G>A (p.Arg461Gln)	rs200140363	0.00002
NM_001006657.2(WDR35):c.1195-2A>T
NM_020779.4(WDR35):c.1255+1G>C	rs371669862
NM_020779.4(WDR35):c.1525-2A>T
NM_020779.4(WDR35):c.1846-30_1848del	rs1553317813
NM_020779.4(WDR35):c.206G>A (p.Gly69Asp)	rs765513105
NM_020779.4(WDR35):c.504T>A (p.Ser168Arg)	rs397515536
NM_020779.4(WDR35):c.570+2T>G

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