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: rs11655081
rs11655081
2 0.923 0.036 17 68386068 intron variant T/C snp 0.18 0.010 < 0.001 1 2015 2015
dbSNP: rs1801968
rs1801968
6 0.878 0.036 9 129818622 missense variant C/G,T snp 0.13; 4.0E-06 0.11 0.010 < 0.001 1 2011 2011
dbSNP: rs587776983
rs587776983
7 0.821 0.214 19 6502209 missense variant G/A,C,T snp 0.010 1.000 1 2014 2014
dbSNP: rs587777074
rs587777074
3 0.878 0.179 19 6495688 missense variant C/T snp 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs767114942
rs767114942
1 1.000 0.036 9 129818826 A/G snp 1.2E-05 6.4E-05 0.010 1.000 1 2015 2015