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 2018
dbSNP: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 5 2009 2013
dbSNP: rs1408272
rs1408272
4 6 25842723 intron variant T/G snv 4.0E-02 0.800 1.000 4 2009 2017
dbSNP: rs218237
rs218237
6 4 54528005 intergenic variant C/T snv 0.18 0.800 1.000 4 2010 2019
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 3 2010 2013
dbSNP: rs2413450
rs2413450
6 22 37074184 intron variant T/C snv 0.61 0.800 1.000 3 2009 2017
dbSNP: rs628751
rs628751
3 6 139517282 intron variant C/A snv 0.41 0.800 1.000 3 2009 2019
dbSNP: rs7776054
rs7776054
13 6 135097778 intron variant A/G snv 0.24 0.800 1.000 3 2009 2018
dbSNP: rs9349205
rs9349205
7 6 41957421 intron variant G/A;C snv 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: rs11085824
rs11085824
4 19 12890733 upstream gene variant A/G snv 0.31 0.800 1.000 2 2009 2017
dbSNP: rs1122794
rs1122794
2 16 259156 intron variant C/A snv 0.19 0.800 1.000 2 2009 2017
dbSNP: rs11915082
rs11915082
2 3 196082268 upstream gene variant G/A snv 0.31 0.800 1.000 2 2009 2017
dbSNP: rs1211375
rs1211375
4 1.000 0.040 16 190281 intron variant A/C;T snv 0.800 1.000 2 2013 2017
dbSNP: rs17342717
rs17342717
8 6 25821542 intron variant C/T snv 6.1E-02 0.800 1.000 2 2010 2012
dbSNP: rs3218097
rs3218097
5 6 41937537 intron variant G/A;T snv 0.800 1.000 2 2010 2012
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: rs6494537
rs6494537
2 15 65759007 intron variant C/G;T snv 0.800 1.000 2 2010 2012
dbSNP: rs6569992
rs6569992
4 6 135131014 intergenic variant G/A;C;T snv 0.800 1.000 2 2010 2012
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: rs855788
rs855788
4 22 37078039 intron variant G/A snv 0.51 0.800 1.000 2 2012 2019
dbSNP: rs668459
rs668459
5 6 139514552 intron variant C/T snv 0.51 0.800 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.800 1.000 1 2013 2013
dbSNP: rs1047891
rs1047891
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 3 2016 2019
dbSNP: rs1434282
rs1434282
6 1 199041592 non coding transcript exon variant C/T snv 0.76 0.700 1.000 3 2016 2019