Gene: SLC22A11 ×
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: rs2078267
rs2078267
SLC22A11
3 0.925 0.120 11 64566642 non coding transcript exon variant C/T snv 0.37 0.800 1.000 6 2009 2019
dbSNP: rs17300741
rs17300741
SLC22A11
3 0.925 0.120 11 64563990 intron variant A/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs17372915
rs17372915
SLC22A11
3 0.925 0.120 11 64564096 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1783811
rs1783811
SLC22A11
3 0.925 0.120 11 64565824 non coding transcript exon variant A/G snv 0.73 0.700 1.000 1 2009 2009
dbSNP: rs3759053
rs3759053
SLC22A11
3 0.925 0.120 11 64555608 upstream gene variant C/T snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs3782099
rs3782099
SLC22A11
3 0.925 0.120 11 64560238 intron variant T/C snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs71456318
rs71456318
SLC22A11
1 11 64565390 non coding transcript exon variant A/C snv 0.39 0.37 0.700 1.000 1 2019 2019
dbSNP: rs7940321
rs7940321
SLC22A11
3 0.925 0.120 11 64556648 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7943154
rs7943154
SLC22A11
3 0.925 0.120 11 64560372 intron variant A/G snv 0.42 0.700 1.000 1 2009 2009