Gene: SLC22A3 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1018234
rs1018234
SLC22A3
1 6 160375026 intron variant C/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs12204009
rs12204009
SLC22A3
1 6 160378214 intron variant T/C snv 2.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs141463285
rs141463285
SLC22A3
1 6 160417614 intron variant T/A snv 4.2E-03 0.700 1.000 1 2017 2017
dbSNP: rs143665477
rs143665477
SLC22A3
1 6 160446240 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs149302195
rs149302195
SLC22A3
1 6 160382662 intron variant C/T snv 2.5E-03 0.700 1.000 1 2017 2017
dbSNP: rs2457574
rs2457574
SLC22A3
1 6 160447669 intron variant G/A snv 0.44 0.42 0.700 1.000 1 2017 2017
dbSNP: rs520829
rs520829
SLC22A3
1 6 160346873 upstream gene variant T/G snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs7769879
rs7769879
SLC22A3
1 6 160444613 intron variant G/C snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs78439586
rs78439586
SLC22A3
1 6 160399890 intron variant G/A;T snv 0.700 1.000 1 2017 2017