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: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2012 2012
dbSNP: rs2301436
rs2301436
11 0.752 0.320 6 167024500 intron variant C/T snv 0.42 0.010 1.000 1 2011 2011
dbSNP: rs3093023
rs3093023
7 0.851 0.160 6 167120802 intron variant G/A snv 0.34 0.010 < 0.001 1 2011 2011
dbSNP: rs3901533
rs3901533
6 0.827 0.280 12 10124484 intron variant A/C snv 0.66 0.010 1.000 1 2019 2019
dbSNP: rs7309123
rs7309123
8 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019