ClinVar Miner

List of variants in gene MIP reported as uncertain significance by Dept. Genetics and Cancer, Menzies Institute for Medical Research, University of Tasmania

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_012064.4(MIP):c.490G>A (p.Val164Ile)	rs149279854	0.00011
NM_012064.4(MIP):c.338G>A (p.Arg113Gln)	rs774928445	0.00001

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