List of variants reported as benign for congenital stationary night blindness 1B

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.1308T>C (p.Thr436=)	rs4701014	0.98353
NM_000843.4(GRM6):c.1131C>T (p.Asp377=)	rs2071246	0.74455
NM_000843.4(GRM6):c.1500+23A>G	rs2256966	0.57932
NM_000843.4(GRM6):c.176A>C (p.Gln59Pro)	rs2645329	0.57334
NM_000843.4(GRM6):c.1392A>G (p.Gly464=)	rs11746675	0.57251
NM_000843.4(GRM6):c.1353T>C (p.Asn451=)	rs2067011	0.50613
NM_000843.4(GRM6):c.1227C>T (p.Tyr409=)	rs2645339	0.49941
NM_000843.4(GRM6):c.2196G>A (p.Thr732=)	rs2071247	0.18181
NM_000843.4(GRM6):c.1533C>T (p.His511=)	rs61733043	0.00512

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