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: rs855791
rs855791
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.800 1.000 7 2010 2019
dbSNP: rs140522
rs140522
11 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 0.800 1.000 5 2012 2018
dbSNP: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 1.000 4 2009 2012
dbSNP: rs218237
rs218237
6 4 54528005 intergenic variant C/T snv 0.18 0.800 1.000 4 2010 2019
dbSNP: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 4 2009 2013
dbSNP: rs9310736
rs9310736
4 3 24309320 intron variant A/G snv 0.69 0.800 1.000 4 2010 2017
dbSNP: rs9349205
rs9349205
7 6 41957421 intron variant G/A;C snv 0.800 1.000 4 2009 2018
dbSNP: rs2236496
rs2236496
5 9 4844265 intron variant T/C snv 0.19 0.800 1.000 3 2010 2013
dbSNP: rs3218097
rs3218097
5 6 41937537 intron variant G/A;T snv 0.800 1.000 3 2010 2013
dbSNP: rs9399137
rs9399137
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.800 1.000 3 2009 2018
dbSNP: rs10758658
rs10758658
4 9 4856877 intron variant G/A snv 0.15 0.800 1.000 2 2009 2017
dbSNP: rs172629
rs172629
2 4 54541595 intergenic variant C/G snv 0.17 0.800 1.000 2 2009 2010
dbSNP: rs2413450
rs2413450
6 22 37074184 intron variant T/C snv 0.61 0.800 1.000 2 2009 2017
dbSNP: rs4820268
rs4820268
14 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 0.800 1.000 2 2009 2012
dbSNP: rs4895441
rs4895441
10 0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 0.800 1.000 2 2009 2012
dbSNP: rs632057
rs632057
5 6 139512875 intron variant T/G snv 0.57 0.800 1.000 2 2010 2012
dbSNP: rs643381
rs643381
4 6 139518286 intron variant C/A;G snv 0.800 1.000 2 2009 2017
dbSNP: rs6569992
rs6569992
4 6 135131014 intergenic variant G/A;C;T snv 0.800 1.000 2 2010 2012
dbSNP: rs668459
rs668459
5 6 139514552 intron variant C/T snv 0.51 0.800 1.000 2 2012 2013
dbSNP: rs7203560
rs7203560
7 1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 0.800 1.000 2 2013 2017
dbSNP: rs7255045
rs7255045
2 19 12821455 intron variant G/A snv 0.37 0.800 1.000 2 2009 2017
dbSNP: rs9374080
rs9374080
2 6 109295217 intron variant T/C snv 0.40 0.800 1.000 2 2009 2017
dbSNP: rs9494145
rs9494145
11 0.925 0.080 6 135111414 intergenic variant T/A;C snv 0.800 1.000 2 2010 2012
dbSNP: rs9859260
rs9859260
2 3 196073676 intron variant C/A;T snv 0.800 1.000 2 2009 2017
dbSNP: rs11239550
rs11239550
3 10 45529281 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009