Here you could input region, variant, rsid or refgene you are interested again.

Example-Region:22:42126499-42130810, Y:9460000-9480000, Variant:10-94780653-G-A, 22-42128945-C-T, Y-9467257-G-A, Rsid:rs4986893, rs3892097, Gene ID:CYP2D6

Search: 22:42126499-42130810

Result

Variant ID	dbSNP	Region	Gene ID	Exonic function	Consequence	Allele Count	Allele Number	Allele Frequency
22-42126578-C-T	-	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.G1337A:p.R446H,CYP2D6:NM_000106:exon9:c.G1490A:p.R497H	1	5982	1.6717e-4
22-42126579-G-A	rs370580423	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.C1336T:p.R446C,CYP2D6:NM_000106:exon9:c.C1489T:p.R497C	1	5982	1.6717e-4
22-42126585-C-T	-	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.G1330A:p.V444M,CYP2D6:NM_000106:exon9:c.G1483A:p.V495M	1	5978	1.6728e-4
22-42126611-C-G	rs1135840	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.G1304C:p.S435T,CYP2D6:NM_000106:exon9:c.G1457C:p.S486T	4193	5972	0.7021
22-42126658-A-G	rs1135836	exonic	CYP2D6;CYP2D7	synonymous SNV	CYP2D6:NM_001025161:exon8:c.T1257C:p.T419T,CYP2D6:NM_000106:exon9:c.T1410C:p.T470T	1	5970	1.6750e-4
22-42126660-T-C	rs1135835	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.A1255G:p.T419A,CYP2D6:NM_000106:exon9:c.A1408G:p.T470A	1	5970	1.6750e-4
22-42126663-G-C	rs1135833	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.C1252G:p.P418A,CYP2D6:NM_000106:exon9:c.C1405G:p.P469A	1	5970	1.6750e-4
22-42126667-C-G	rs1135832	exonic	CYP2D6;CYP2D7	synonymous SNV	CYP2D6:NM_001025161:exon8:c.G1248C:p.S416S,CYP2D6:NM_000106:exon9:c.G1401C:p.S467S	2	5970	3.3501e-4
22-42126712-C-T	-	exonic	CYP2D6;CYP2D7	synonymous SNV	CYP2D6:NM_001025161:exon8:c.G1203A:p.E401E,CYP2D6:NM_000106:exon9:c.G1356A:p.E452E	1	5982	1.6717e-4
22-42126746-C-T	rs532668079	exonic	CYP2D6;CYP2D7	nonsynonymous SNV	CYP2D6:NM_001025161:exon8:c.G1169A:p.R390H,CYP2D6:NM_000106:exon9:c.G1322A:p.R441H	3	5982	5.0150e-4