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: rs7775698
rs7775698
12 1.000 0.071 6 135097497 intron variant C/T snp 4.4E-02; 3.2E-05 0.800 6 2009 2013
dbSNP: rs855791
rs855791
26 0.715 0.393 22 37066896 missense variant A/G,T snp 0.57; 4.0E-06 0.65 0.800 6 2010 2017
dbSNP: rs1122794
rs1122794
4 1.000 16 259156 intron variant C/A snp 0.18 0.800 4 2009 2017
dbSNP: rs1408272
rs1408272
5 6 25842723 intron variant T/G snp 3.9E-02 0.800 4 2009 2017
dbSNP: rs1800562
rs1800562
175 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 0.800 4 2011 2013
dbSNP: rs218237
rs218237
7 4 54528005 intergenic variant C/T snp 0.18 0.800 4 2010 2017
dbSNP: rs2413450
rs2413450
7 22 37074184 intron variant T/C snp 0.61 0.800 4 2009 2017
dbSNP: rs4820268
rs4820268
12 0.846 0.143 22 37073551 synonymous variant G/A,C snp 0.53; 4.0E-06 0.59 0.800 4 2009 2012
dbSNP: rs1050828
rs1050828
12 0.846 0.143 X 154536002 missense variant C/T snp 9.1E-03 3.2E-02 0.800 3 2013 2017
dbSNP: rs10758658
rs10758658
4 9 4856877 intron variant G/A snp 0.17 0.800 3 2009 2017
dbSNP: rs11085824
rs11085824
5 19 12890733 regulatory region variant A/G snp 0.30 0.800 3 2009 2017
dbSNP: rs11915082
rs11915082
2 3 196082268 regulatory region variant G/A snp 0.30 0.800 3 2009 2017
dbSNP: rs17342717
rs17342717
5 6 25821542 intron variant C/T snp 6.5E-02 0.800 3 2011 2012
dbSNP: rs218265
rs218265
12 4 54542832 regulatory region variant T/C snp 0.20 0.800 3 2012 2017
dbSNP: rs2572207
rs2572207
3 15 65778355 intron variant C/A,T snp 0.32 0.800 3 2012 2017
dbSNP: rs3218097
rs3218097
6 6 41937537 intron variant G/A,T snp 0.21 0.800 3 2010 2012
dbSNP: rs592423
rs592423
7 6 139519556 intergenic variant A/C snp 0.49 0.800 3 2012 2017
dbSNP: rs6569992
rs6569992
5 6 135131014 intergenic variant G/A,C,T snp 0.18; 9.6E-05 0.800 3 2011 2012
dbSNP: rs7776054
rs7776054
15 6 135097778 intron variant A/G snp 0.26 0.800 3 2009 2017
dbSNP: rs9349205
rs9349205
5 6 41957421 intron variant G/A,C snp 0.18 0.800 3 2009 2017
dbSNP: rs10758656
rs10758656
4 9 4852599 intron variant A/G snp 0.20 0.800 2 2012 2017
dbSNP: rs10849023
rs10849023
4 12 4223312 regulatory region variant C/T snp 0.22 0.800 2 2012 2017
dbSNP: rs11211480
rs11211480
2 1 47227548 non coding transcript exon variant A/G snp 0.44 0.800 2 2012 2017
dbSNP: rs11239550
rs11239550
3 10 45529281 intron variant A/G snp 0.32 0.800 2 2012 2017
dbSNP: rs11811522
rs11811522
2 1 158634353 intron variant G/A snp 0.34 0.800 2 2012 2017