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: rs715505
rs715505
1 1.000 0.080 22 39355246 intron variant G/C snv 0.21 0.700 1.000 2 2012 2012
dbSNP: rs72678531
rs72678531
1 1.000 0.080 1 67332762 intron variant T/C snv 0.17 0.800 1.000 2 2012 2012
dbSNP: rs7665090
rs7665090
1 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.800 1.000 2 2011 2012
dbSNP: rs8067378
rs8067378
6 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 0.800 1.000 2 2012 2012
dbSNP: rs907091
rs907091
3 0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 0.700 1.000 2 2012 2012
dbSNP: rs911263
rs911263
1 0.851 0.200 14 68286876 intron variant C/T snv 0.57 0.800 1.000 2 2011 2015
dbSNP: rs1003643
rs1003643
1 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs1003644
rs1003644
1 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs1005999
rs1005999
1 1.000 0.080 2 104907333 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1008591
rs1008591
1 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1008723
rs1008723
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1011082
rs1011082
1 1.000 0.080 17 39912261 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1015092
rs1015092
1 1.000 0.080 20 8769415 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1019212
rs1019212
1 1.000 0.080 19 46225962 upstream gene variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10234405
rs10234405
1 1.000 0.080 7 4034827 intron variant A/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10237319
rs10237319
1 1.000 0.080 7 4033969 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10237488
rs10237488
1 1.000 0.080 7 4034710 intron variant T/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10237838
rs10237838
1 1.000 0.080 7 4034366 intron variant C/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs10265937
rs10265937
1 1.000 0.080 7 4034017 intron variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs10266101
rs10266101
1 1.000 0.080 7 4034187 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10278187
rs10278187
1 1.000 0.080 7 4034741 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1031458
rs1031458
1 1.000 0.080 17 39915920 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10445308
rs10445308
3 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10445337
rs10445337
3 0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 0.700 1.000 1 2012 2012
dbSNP: rs10445371
rs10445371
3 0.925 0.120 17 45988044 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012