List of variants in gene CSF3R reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000760.4(CSF3R):c.1213G>A (p.Glu405Lys)	rs3918019	0.00492
NM_000760.4(CSF3R):c.447G>C (p.Glu149Asp)	rs139332126	0.00300
NM_000760.4(CSF3R):c.2041-30C>T	rs3918021	0.00270
NM_000760.4(CSF3R):c.108C>T (p.Val36=)	rs3918011	0.00193
NM_000760.4(CSF3R):c.1856T>C (p.Leu619Ser)	rs141619366	0.00115
NM_000760.4(CSF3R):c.2211C>T (p.Ser737=)	rs376211630	0.00034
NM_000760.4(CSF3R):c.1761C>T (p.Leu587=)	rs149239453	0.00014
NM_000760.4(CSF3R):c.885C>T (p.Cys295=)	rs747273831	0.00008
NM_000760.4(CSF3R):c.1900G>A (p.Gly634Ser)
NM_000760.4(CSF3R):c.2041-35T>C
NM_000760.4(CSF3R):c.569G>A (p.Arg190His)

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