ClinVar Miner

List of variants in gene GFM1 reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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_024996.7(GFM1):c.607A>G (p.Ile203Val)	rs1722079229	0.00001
NM_024996.7(GFM1):c.881C>T (p.Pro294Leu)	rs1722451256

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