List of variants in gene GRID2 reported as uncertain significance by GeneDx

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_001510.4(GRID2):c.2032C>G (p.Pro678Ala)	rs146342092	0.00077
NM_001510.4(GRID2):c.1946C>T (p.Thr649Met)	rs150683134	0.00011
NM_001510.4(GRID2):c.587C>A (p.Ala196Glu)	rs192450353	0.00007
NM_001510.4(GRID2):c.899G>A (p.Arg300His)	rs201635818	0.00002
NM_001510.4(GRID2):c.950C>T (p.Ala317Val)	rs538573274	0.00001
GRCh37/hg19 4q22.2(chr4:94015225-94113162)x1
NM_001510.4(GRID2):c.1178A>G (p.Asn393Ser)	rs1085307659
NM_001510.4(GRID2):c.1412C>G (p.Ser471Cys)
NM_001510.4(GRID2):c.1945A>T (p.Thr649Ser)	rs2546697844
NM_001510.4(GRID2):c.1948G>C (p.Ala650Pro)	rs2149459950
NM_001510.4(GRID2):c.2490C>A (p.Ser830Arg)

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