Gene: SLC22A12 ×
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: rs10897518
rs10897518
SLC22A12
3 0.925 0.120 11 64593233 intron variant C/T snv 0.51 0.700 1.000 2 2010 2013
dbSNP: rs11231825
rs11231825
SLC22A12
5 0.827 0.240 11 64592802 synonymous variant T/C snv 0.57 0.51 0.700 1.000 2 2010 2013
dbSNP: rs3825016
rs3825016
SLC22A12
3 0.882 0.160 11 64591814 synonymous variant C/T snv 0.57 0.51 0.700 1.000 2 2010 2013
dbSNP: rs3825018
rs3825018
SLC22A12
2 0.925 0.120 11 64591337 5 prime UTR variant G/A snv 0.51 0.700 1.000 2 2010 2013
dbSNP: rs475688
rs475688
SLC22A12
3 0.882 0.160 11 64596819 intron variant C/T snv 0.25 0.700 1.000 2 2010 2013
dbSNP: rs505802
rs505802
SLC22A12
4 0.882 0.160 11 64589600 upstream gene variant T/C snv 0.45 0.700 1.000 2 2010 2013
dbSNP: rs524023
rs524023
SLC22A12
2 0.925 0.120 11 64590793 5 prime UTR variant C/G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs893006
rs893006
SLC22A12
3 0.882 0.160 11 64598324 intron variant C/A snv 0.61 0.700 1.000 2 2010 2013
dbSNP: rs9734313
rs9734313
SLC22A12
2 0.925 0.120 11 64590839 5 prime UTR variant C/G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs12800450
rs12800450
SLC22A12
3 0.925 0.120 11 64591749 missense variant G/A;T snv 0.700 1.000 1 2011 2011