List of variants in gene GRM6 reported by Retina International

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.176A>C (p.Gln59Pro)	rs2645329	0.57334
NM_000843.4(GRM6):c.504+66A>C	rs62638203	0.02083
NM_000843.4(GRM6):c.352C>A (p.Arg118Ser)	rs62638201	0.01102
NM_000843.4(GRM6):c.19G>A (p.Ala7Thr)	rs62642053	0.00533
NM_000843.4(GRM6):c.733A>G (p.Ile245Val)	rs62638207	0.00147
NM_000843.4(GRM6):c.261C>T (p.Pro87=)	rs62638199	0.00032
NM_000843.4(GRM6):c.137C>T (p.Pro46Leu)	rs62638197	0.00009
NM_000843.4(GRM6):c.721+83G>T	rs62638206	0.00006
NM_000843.4(GRM6):c.448G>A (p.Gly150Ser)	rs62638202	0.00003
NM_000843.4(GRM6):c.664G>A (p.Glu222Lys)	rs62638204	0.00003
NM_000843.4(GRM6):c.172G>C (p.Gly58Arg)	rs62638198
NM_000843.4(GRM6):c.336C>T (p.Phe112=)	rs62638200
NM_000843.4(GRM6):c.57_75dup (p.Leu26fs)	rs281865185
NM_000843.4(GRM6):c.686G>A (p.Gly229Glu)	rs62638205
NM_000843.4(GRM6):c.727G>T (p.Val243Phe)	rs17078894
NM_000843.4(GRM6):c.727dup	rs281865186
NM_000843.4(GRM6):c.83G>A (p.Arg28His)	rs62638196

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