List of variants in gene GDI1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001493.3(GDI1):c.771C>T (p.Asp257=)	rs200964754	0.00044
NM_001493.3(GDI1):c.696C>T (p.Gly232=)	rs146653767	0.00026
NM_001493.3(GDI1):c.1167C>T (p.Pro389=)	rs140855833	0.00022
NM_001493.3(GDI1):c.102C>T (p.Asp34=)	rs1172499879	0.00002
NM_001493.3(GDI1):c.471C>T (p.Thr157=)	rs782808997	0.00001
NM_001493.2(GDI1):c.-114C>T
NM_001493.3(GDI1):c.1203C>G (p.Ser401=)
NM_001493.3(GDI1):c.156G>C (p.Leu52=)
NM_001493.3(GDI1):c.558C>T (p.Gly186=)
NM_001493.3(GDI1):c.714T>C (p.Phe238=)
NM_001493.3(GDI1):c.827G>A (p.Arg276His)

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