List of variants in gene CSF1R reported as uncertain significance for Brain abnormalities, neurodegeneration, and dysosteosclerosis

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001288705.3(CSF1R):c.110C>T (p.Thr37Met)	rs139635308	0.00018
NM_001288705.3(CSF1R):c.1402G>T (p.Val468Leu)	rs756493296	0.00002
NM_001288705.3(CSF1R):c.349G>A (p.Val117Met)	rs566891025	0.00001
NM_001288705.3(CSF1R):c.2308G>A (p.Ala770Thr)
NM_001288705.3(CSF1R):c.2517G>T (p.Trp839Cys)	rs1757199923
NM_001288705.3(CSF1R):c.2809A>G (p.Ser937Gly)
NM_001288705.3(CSF1R):c.604C>T (p.Pro202Ser)
NM_001288705.3(CSF1R):c.740C>T (p.Pro247Leu)

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