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

items per page

Total page: 23   Total amount: 229

Variant ID
dbSNP
Region
Gene ID
Exonic
function
Consequence
Allele
Count
Allele
Number
Allele
Frequency
rs376446555
ncRNA_exonic
LOC101929829
-
-
3
5980
5.0167e-4
rs369385518
ncRNA_exonic
LOC101929829
-
-
3
5980
5.0167e-4
rs766720823
ncRNA_exonic
LOC101929829
-
-
3
5978
5.0184e-4
rs773790593
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.C14T:p.A5V,CYP2D6:NM_001025161:exon1:c.C14T:p.A5V
2
5978
3.3456e-4
rs769258
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.G31A:p.V11M,CYP2D6:NM_001025161:exon1:c.G31A:p.V11M
8
5978
1.3382e-3
rs138417770
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.G74A:p.R25Q,CYP2D6:NM_001025161:exon1:c.G74A:p.R25Q
2
5978
3.3456e-4
rs28371696
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.G77A:p.R26H,CYP2D6:NM_001025161:exon1:c.G77A:p.R26H
3
5978
5.0184e-4
rs1065852
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.C100T:p.P34S,CYP2D6:NM_001025161:exon1:c.C100T:p.P34S
3147
5976
0.5266
-
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.T119G:p.L40R,CYP2D6:NM_001025161:exon1:c.T119G:p.L40R
2
5976
3.3467e-4
rs118203758
exonic
CYP2D6;CYP2D7
nonsynonymous SNV
CYP2D6:NM_000106:exon1:c.G125A:p.G42E,CYP2D6:NM_001025161:exon1:c.G125A:p.G42E
6
5976
1.0040e-3
Total page: 23   Total amount: 229