List of variants in gene WDR26 reported as uncertain significance for Inborn genetic diseases

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001379403.1(WDR26):c.2267G>T (p.Cys756Phe)	rs1553350638	0.00001
NM_001379403.1(WDR26):c.1073T>C (p.Met358Thr)
NM_001379403.1(WDR26):c.1441A>G (p.Ile481Val)
NM_001379403.1(WDR26):c.1457C>T (p.Pro486Leu)
NM_001379403.1(WDR26):c.1458+3A>G
NM_001379403.1(WDR26):c.1669G>C (p.Asp557His)
NM_001379403.1(WDR26):c.1812T>A (p.Asp604Glu)	rs528360727
NM_001379403.1(WDR26):c.1870C>G (p.Gln624Glu)	rs1553353230
NM_001379403.1(WDR26):c.1888A>T (p.Met630Leu)
NM_001379403.1(WDR26):c.311A>G (p.Asn104Ser)
NM_001379403.1(WDR26):c.410C>T (p.Ala137Val)
NM_001379403.1(WDR26):c.425C>G (p.Ser142Trp)
NM_001379403.1(WDR26):c.471T>G (p.Asn157Lys)
NM_001379403.1(WDR26):c.559G>T (p.Ala187Ser)
NM_001379403.1(WDR26):c.566C>T (p.Ser189Leu)	rs1558450796
NM_001379403.1(WDR26):c.586T>G (p.Ser196Ala)
NM_001379403.1(WDR26):c.598G>A (p.Ala200Thr)
NM_001379403.1(WDR26):c.652A>C (p.Lys218Gln)

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