List of variants in gene GRM6 reported as pathogenic for perceptual disorders

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.137C>T (p.Pro46Leu)	rs62638197	0.00009
NM_000843.4(GRM6):c.448G>A (p.Gly150Ser)	rs62638202	0.00003
NM_000843.3(GRM6):c.(1354+1_1355-1)_(2436+1_2437-1)del
NM_000843.4(GRM6):c.577del (p.Val193fs)	rs781463257
NM_000843.4(GRM6):c.722-1G>T	rs766594761
NM_000843.4(GRM6):c.727dup	rs281865186

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