List of variants in gene GORAB reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_152281.3(GORAB):c.-21G>A	rs149401558	0.00008
NM_152281.3(GORAB):c.952G>A (p.Val318Met)	rs199673882	0.00006
NM_152281.3(GORAB):c.223G>A (p.Val75Ile)	rs751708902	0.00004
NM_152281.3(GORAB):c.782T>A (p.Leu261His)	rs773952908	0.00003
NM_152281.3(GORAB):c.648C>G (p.Asp216Glu)	rs780332229	0.00001
NM_152281.3(GORAB):c.662G>A (p.Arg221Gln)	rs773728833	0.00001
NM_152281.3(GORAB):c.790G>T (p.Ala264Ser)	rs760576900	0.00001
NM_152281.3(GORAB):c.805G>A (p.Glu269Lys)	rs765224001	0.00001
NM_152281.3(GORAB):c.88C>G (p.Pro30Ala)

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