ClinVar Miner

List of variants in gene GDF11 reported as uncertain significance by Undiagnosed Diseases Network, NIH

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_005811.5(GDF11):c.916G>A (p.Glu306Lys)	rs1444997099	0.00001
NM_005811.5(GDF11):c.1008C>G (p.Tyr336Ter)	rs1449282134

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