List of variants in gene CSF1R reported as likely pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001288705.3(CSF1R):c.1711T>G (p.Tyr571Asp)	rs1057519802
NM_001288705.3(CSF1R):c.2905T>C (p.Tyr969His)	rs121913393
NM_001288705.3(CSF1R):c.2906A>G (p.Tyr969Cys)	rs1801271
NM_001288705.3(CSF1R):c.2906A>T (p.Tyr969Phe)	rs1801271
NM_001288705.3(CSF1R):c.902T>C (p.Leu301Ser)	rs121913390
NM_001288705.3(CSF1R):c.903G>T (p.Leu301Phe)	rs1057520014

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