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: rs1801968
rs1801968
7 0.827 0.040 9 129818622 missense variant C/G;T snv 0.13; 4.0E-06 0.020 0.500 2 2012 2013
dbSNP: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.020 < 0.001 2 2013 2014
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.020 < 0.001 2 2013 2014
dbSNP: rs1182
rs1182
9 0.790 0.160 9 129813781 3 prime UTR variant C/A snv 0.17 0.010 1.000 1 2012 2012
dbSNP: rs587776983
rs587776983
9 0.807 0.240 19 6502209 missense variant G/A;C;T snv 0.010 1.000 1 2014 2014