Gene: SLC22A4 ×
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: rs3792876
rs3792876
SLC22A4
7 0.790 0.280 5 132301616 intron variant C/T snv 6.9E-02 0.040 0.500 4 2005 2015
dbSNP: rs2073838
rs2073838
SLC22A4 ; MIR3936HG
1 1.000 0.120 5 132313529 intron variant G/A snv 7.0E-02 0.020 0.500 2 2008 2015
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
10 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2008 2008