List of variants in gene GIMD1 reported as uncertain significance by Ambry Genetics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001195138.2(GIMD1):c.136T>C (p.Cys46Arg)	rs963071670	0.00002
NM_001195138.2(GIMD1):c.167A>C (p.His56Pro)	rs1025096884	0.00001
NM_001195138.2(GIMD1):c.178C>T (p.Arg60Cys)	rs779850471
NM_001195138.2(GIMD1):c.541T>C (p.Tyr181His)	rs2476260942

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