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: rs7869487
rs7869487
3 0.882 0.040 9 114818634 intergenic variant C/G;T snv 0.830 1.000 5 2005 2015
dbSNP: rs4263839
rs4263839
7 0.807 0.160 9 114804160 intron variant A/G snv 0.75 0.830 0.750 4 2008 2014
dbSNP: rs4409764
rs4409764
3 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 0.820 1.000 5 2010 2019
dbSNP: rs1250550
rs1250550
5 0.851 0.240 10 79300560 intron variant C/A snv 0.27 0.820 1.000 4 2010 2017
dbSNP: rs2872507
rs2872507
12 0.752 0.360 17 39884510 intergenic variant G/A;T snv 0.820 1.000 4 2008 2016
dbSNP: rs9271366
rs9271366
9 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 0.820 1.000 4 2011 2015
dbSNP: rs11175593
rs11175593
3 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 0.820 1.000 3 2008 2013
dbSNP: rs11747270
rs11747270
7 0.790 0.240 5 150879305 intron variant A/G snv 0.21 0.820 0.667 3 2008 2020
dbSNP: rs6478106
rs6478106
2 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 0.820 1.000 3 2005 2019
dbSNP: rs212388
rs212388
8 0.827 0.240 6 159069404 intron variant C/G;T snv 0.810 1.000 6 2010 2017
dbSNP: rs6651252
rs6651252
8 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.810 1.000 6 2010 2019
dbSNP: rs3764147
rs3764147
7 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 0.810 1.000 5 2008 2017
dbSNP: rs10761659
rs10761659
3 0.925 0.040 10 62685804 intron variant A/G snv 0.43 0.810 1.000 4 2010 2017
dbSNP: rs2188962
rs2188962
5 0.882 0.160 5 132435113 intron variant C/T snv 0.29 0.810 1.000 4 2008 2017
dbSNP: rs2301436
rs2301436
11 0.752 0.320 6 167024500 intron variant C/T snv 0.42 0.810 1.000 4 2008 2016
dbSNP: rs7746082
rs7746082
5 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 0.810 1.000 4 2008 2017
dbSNP: rs9858542
rs9858542
BSN
3 0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 0.810 1.000 4 2007 2010
dbSNP: rs10045431
rs10045431
4 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.810 1.000 3 2008 2014
dbSNP: rs11805303
rs11805303
6 0.827 0.240 1 67209833 intron variant C/T snv 0.30 0.810 1.000 3 2007 2012
dbSNP: rs17221417
rs17221417
3 0.925 0.040 16 50705671 intron variant C/G snv 0.20 0.810 1.000 3 2007 2017
dbSNP: rs17234657
rs17234657
3 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 0.810 1.000 3 2007 2010
dbSNP: rs224136
rs224136
2 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 0.810 0.667 3 2007 2019
dbSNP: rs5743289
rs5743289
2 1.000 0.040 16 50722863 intron variant C/G;T snv 0.810 1.000 3 2007 2014
dbSNP: rs10210302
rs10210302
1 1.000 0.040 2 233250193 intron variant C/A;T snv 0.810 1.000 2 2007 2010
dbSNP: rs102275
rs102275
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.810 1.000 2 2010 2018