ClinVar Miner

List of variants in gene SMG9 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_019108.4(SMG9):c.490C>T (p.Pro164Ser)	rs143775531	0.00001
NM_019108.4(SMG9):c.611T>A (p.Val204Glu)	rs778572007

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