List of variants in gene GRM1 reported as uncertain significance for cerebellar disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001278064.2(GRM1):c.1073G>A (p.Arg358Lys)	rs112817798	0.00024
NM_001278064.2(GRM1):c.1165A>C (p.Asn389His)	rs769064791	0.00007
NM_001278064.2(GRM1):c.827A>C (p.Lys276Thr)	rs192397712	0.00006
NM_001278064.2(GRM1):c.2909C>T (p.Pro970Leu)	rs1432380664	0.00003
NM_001278064.2(GRM1):c.3236C>T (p.Pro1079Leu)	rs145216301	0.00001
NM_001278064.2(GRM1):c.3405C>G (p.Ser1135Arg)	rs1188689970	0.00001
NM_001278064.2(GRM1):c.951-6T>A	rs758215901	0.00001
NM_001278064.2(GRM1):c.2867A>T (p.Asn956Ile)	rs1212150882
NM_001278064.2(GRM1):c.829C>A (p.Leu277Ile)	rs1022097029
NM_001278064.2(GRM1):c.851C>T (p.Ala284Val)	rs1448466753

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