List of variants in gene CSF3R 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)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000760.4(CSF3R):c.1640G>A (p.Trp547Ter)	rs138156467	0.00026
NM_000760.4(CSF3R):c.340C>T (p.Gln114Ter)	rs756667927	0.00001
NM_000760.4(CSF3R):c.1576+1G>A	rs1031224658
NM_000760.4(CSF3R):c.1577-1G>A
NM_000760.4(CSF3R):c.1843A>G (p.Thr615Ala)	rs1057519776
NM_000760.4(CSF3R):c.1853C>T (p.Thr618Ile)	rs796065343
NM_000760.4(CSF3R):c.361+1G>T
NM_000760.4(CSF3R):c.65-1G>A
NM_000760.4(CSF3R):c.65-2A>C
NM_000760.4(CSF3R):c.843+2T>C	rs1650834071
NM_000760.4(CSF3R):c.922C>T (p.Arg308Cys)	rs606231473
NM_000760.4(CSF3R):c.998-1G>A	rs1248511242
NM_000760.4(CSF3R):c.998-2A>T	rs879253750

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