List of variants in gene GRM7 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000844.4(GRM7):c.519+7A>G	rs342034	0.96844
NM_000844.4(GRM7):c.2196T>C (p.Tyr732=)	rs1485175	0.56650
NM_000844.4(GRM7):c.222C>T (p.Asn74=)	rs3749380	0.37363
NM_000844.4(GRM7):c.1298A>T (p.Tyr433Phe)	rs2229902	0.30241
NM_000844.4(GRM7):c.1789C>T (p.Leu597=)	rs7614915	0.22935
NM_000844.4(GRM7):c.1575A>G (p.Leu525=)	rs34373930	0.22930
NM_000844.4(GRM7):c.2235G>A (p.Gly745=)	rs1485174	0.22896
NM_000844.4(GRM7):c.2698+15G>A	rs2280739	0.12153
NM_000844.4(GRM7):c.99C>A (p.Arg33=)	rs116111799	0.01523
NM_000844.4(GRM7):c.1750C>T (p.Leu584=)	rs80099685	0.01295
NM_000844.4(GRM7):c.561T>C (p.Ser187=)	rs35106713	0.00841
NM_000844.4(GRM7):c.2439A>G (p.Gln813=)	rs76544064	0.00723
NM_000844.4(GRM7):c.552C>A (p.Pro184=)	rs139429824	0.00484
NM_000844.4(GRM7):c.1179G>A (p.Gln393=)	rs34067965	0.00405
NM_000844.4(GRM7):c.81G>C (p.Ala27=)	rs138762445	0.00300
NM_000844.4(GRM7):c.144C>T (p.Asp48=)	rs142650646	0.00153
NM_000844.4(GRM7):c.2577G>C (p.Arg859=)	rs201806420	0.00090
NM_000844.4(GRM7):c.1854G>A (p.Thr618=)	rs146236743	0.00078
NM_000844.4(GRM7):c.1356A>C (p.Ile452=)	rs138874035	0.00066
NM_000844.4(GRM7):c.114C>T (p.Tyr38=)	rs114869468	0.00063
NM_000844.4(GRM7):c.1026G>A (p.Thr342=)	rs78137319	0.00052
NM_000844.4(GRM7):c.759C>T (p.Ser253=)	rs144380165	0.00041
NM_000844.4(GRM7):c.300G>T (p.Thr100=)	rs555598605	0.00028
NM_000844.4(GRM7):c.2388G>A (p.Thr796=)	rs117160055	0.00020
NM_000844.4(GRM7):c.67G>A (p.Val23Met)	rs535666333	0.00015
NM_000844.4(GRM7):c.2655C>T (p.Asn885=)	rs546761323	0.00006
NM_000844.4(GRM7):c.1175-48TG[16]	rs111752136
NM_000844.4(GRM7):c.1300C>A (p.Arg434=)	rs201868190

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