List of variants in gene VRK1 reported as benign for bulbospinal muscular atrophy

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003384.3(VRK1):c.217-244T>C	rs12586511	0.34167
NM_003384.3(VRK1):c.705C>T (p.Gly235=)	rs2230532	0.32707
NM_003384.3(VRK1):c.45A>G (p.Ala15=)	rs2145635	0.32398
NM_003384.3(VRK1):c.1159+43C>G	rs45457797	0.08564
NM_003384.3(VRK1):c.286+12A>G	rs376603491	0.00085
NM_003384.3(VRK1):c.1020C>T (p.Asp340=)	rs147853760	0.00066
NM_003384.3(VRK1):c.375-8G>C	rs191021502	0.00051
NM_003384.3(VRK1):c.710-13C>T	rs374386994	0.00016
NM_003384.3(VRK1):c.1160-8del	rs2139857568
NM_003384.3(VRK1):c.161-7dup	rs1295596727
NM_003384.3(VRK1):c.374+7dup
NM_003384.3(VRK1):c.375-14A>G
NM_003384.3(VRK1):c.483+20_483+22del	rs566207500

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