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: rs10034228
rs10034228
3 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10053502
rs10053502
1 1.000 0.040 5 39979070 intron variant C/T snv 6.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs10274279
rs10274279
1 1.000 0.040 7 157594749 intron variant T/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs10747502
rs10747502
2 1.000 0.040 1 99058491 intron variant A/G snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs11223996
rs11223996
1 1.000 0.040 11 134756993 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11618212
rs11618212
1 1.000 0.040 13 105444463 intergenic variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs11838472
rs11838472
1 1.000 0.040 13 73167012 regulatory region variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs12032643
rs12032643
1 1.000 0.040 1 248874237 intergenic variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12216812
rs12216812
1 1.000 0.040 8 81239512 upstream gene variant G/A snv 6.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs12525668
rs12525668
1 1.000 0.040 6 107696467 downstream gene variant A/G snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs1302019
rs1302019
1 1.000 0.040 6 147650438 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13172324
rs13172324
1 1.000 0.040 5 7368732 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13382811
rs13382811
4 0.882 0.040 2 144466053 intron variant C/T snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs1472750
rs1472750
1 1.000 0.040 10 113475355 regulatory region variant T/C snv 0.92 0.700 1.000 1 2012 2012
dbSNP: rs1559777
rs1559777
1 1.000 0.040 15 57788419 intergenic variant G/A snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1656966
rs1656966
2 0.925 0.080 3 186748463 intron variant G/A snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs1668357
rs1668357
1 1.000 0.040 7 37964804 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs16862782
rs16862782
1 1.000 0.040 3 187970102 intron variant C/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs16872571
rs16872571
2 0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs17103138
rs17103138
1 1.000 0.040 10 122153815 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs17788937
rs17788937
1 1.000 0.040 12 77505730 intron variant G/A snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs17822114
rs17822114
1 1.000 0.040 16 60699699 intergenic variant C/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17826255
rs17826255
1 1.000 0.040 17 31006498 upstream gene variant T/C snv 4.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs189798
rs189798
1 1.000 0.040 8 9133067 downstream gene variant A/G snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs2730260
rs2730260
1 1.000 0.040 7 159054238 intron variant G/C;T snv 0.700 1.000 1 2013 2013