List of variants in gene GRM4 reported as benign for not provided

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000841.4(GRM4):c.1959G>A (p.Ser653=)	rs34858760	0.02488
NM_000841.4(GRM4):c.2304C>T (p.Thr768=)	rs61745457	0.01673
NM_000841.4(GRM4):c.2712C>T (p.Tyr904=)	rs45558337	0.00484
NM_000841.4(GRM4):c.1713G>A (p.Thr571=)	rs61744332	0.00178
NM_000841.4(GRM4):c.2205C>T (p.Leu735=)	rs150639507	0.00176
NM_000841.4(GRM4):c.1977G>A (p.Leu659=)	rs151333213	0.00148
NM_000841.4(GRM4):c.1447C>T (p.Arg483Cys)	rs188910868	0.00056
NM_000841.4(GRM4):c.2532C>A (p.Ile844=)	rs762697734	0.00030

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