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: rs113352275
rs113352275
2 15 78548225 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs28498264
rs28498264
2 15 78545331 intron variant C/T snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs34138960
rs34138960
2 15 78539326 upstream gene variant A/G;T snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs34664138
rs34664138
2 15 78539282 upstream gene variant T/G snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs35212593
rs35212593
2 15 78539484 upstream gene variant G/A snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs56117933
rs56117933
3 1.000 0.040 15 78540007 upstream gene variant T/C snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs59133824
rs59133824
2 15 78541108 non coding transcript exon variant C/A snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs59683676
rs59683676
2 15 78541111 non coding transcript exon variant T/C snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs905739
rs905739
2 15 78552768 downstream gene variant A/G snv 0.27 0.700 1.000 1 2015 2015