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: rs1205349
rs1205349
2 20 34311868 upstream gene variant G/C snv 0.72 0.700 1.000 1 2010 2010
dbSNP: rs1205350
rs1205350
2 20 34310533 intron variant G/A snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs1205357
rs1205357
2 20 34289960 intron variant C/T snv 0.70 0.700 1.000 1 2010 2010
dbSNP: rs2378132
rs2378132
2 20 34258230 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6088443
rs6088443
2 20 34244325 intron variant C/T snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs6088454
rs6088454
2 20 34266771 intron variant A/T snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs6120580
rs6120580
2 20 34256724 intron variant C/T snv 0.25 0.700 1.000 1 2010 2010
dbSNP: rs819133
rs819133
2 20 34282508 intron variant T/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs819136
rs819136
2 20 34260913 intron variant G/A snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs819142
rs819142
2 20 34273201 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs819144
rs819144
2 20 34273750 intron variant T/G snv 0.75 0.700 1.000 1 2010 2010
dbSNP: rs819145
rs819145
2 20 34274021 intron variant T/G snv 0.75 0.700 1.000 1 2010 2010
dbSNP: rs819146
rs819146
2 20 34303394 intron variant G/T snv 0.71 0.700 1.000 1 2010 2010
dbSNP: rs819147
rs819147
2 20 34301898 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs819148
rs819148
2 20 34300731 intron variant G/A snv 0.71 0.700 1.000 1 2010 2010
dbSNP: rs819156
rs819156
2 20 34293217 intron variant A/C snv 0.87 0.700 1.000 1 2010 2010
dbSNP: rs819158
rs819158
2 20 34292932 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs819159
rs819159
2 20 34291914 intron variant A/T snv 0.71 0.700 1.000 1 2010 2010
dbSNP: rs819162
rs819162
2 20 34264476 intron variant A/T snv 0.25 0.700 1.000 1 2010 2010
dbSNP: rs819163
rs819163
2 20 34254551 intron variant T/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs819164
rs819164
2 20 34251648 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs819172
rs819172
2 20 34279700 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs819173
rs819173
2 20 34278756 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs819175
rs819175
2 20 34278375 intron variant G/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs819176
rs819176
2 20 34278038 intron variant T/A;G snv 0.700 1.000 1 2010 2010