List of variants in gene CSF2RB reported as benign for not specified

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000395.3(CSF2RB):c.1944A>G (p.Pro648=)	rs131840	0.77443
NM_000395.3(CSF2RB):c.1278C>T (p.Ser426=)	rs1801117	0.20636
NM_000395.3(CSF2RB):c.745G>C (p.Glu249Gln)	rs16845	0.10045
NM_000395.3(CSF2RB):c.1569-13T>G	rs16997510	0.06392
NM_000395.3(CSF2RB):c.1954G>A (p.Val652Met)	rs1801114	0.05618
NM_000395.3(CSF2RB):c.702C>T (p.Cys234=)	rs16846	0.04733
NM_000395.3(CSF2RB):c.2086C>T (p.Pro696Ser)	rs16997517	0.04529
NM_000395.3(CSF2RB):c.1807C>A (p.Pro603Thr)	rs1801122	0.03000
NM_000395.3(CSF2RB):c.2400G>A (p.Pro800=)	rs1801116	0.02286
NM_000395.3(CSF2RB):c.2430C>A (p.Pro810=)	rs2228092	0.01431
NM_000395.3(CSF2RB):c.934G>A (p.Asp312Asn)	rs117805308	0.01316
NM_000395.3(CSF2RB):c.1153-13T>C	rs117405606	0.00853
NM_000395.3(CSF2RB):c.1596C>T (p.Ser532=)	rs115580664	0.00495
NM_000395.3(CSF2RB):c.1464+15C>T	rs186445757	0.00153

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