ClinVar Miner

List of variants in gene GLYR1 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_032569.4(GLYR1):c.596C>T (p.Ala199Val)	rs369808296	0.00001
NM_032569.4(GLYR1):c.584G>T (p.Gly195Val)	rs1555500532

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