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: rs10065906
rs10065906
1 1.000 0.040 5 159580770 intron variant C/A snv 0.74 0.800 1.000 1 2013 2013
dbSNP: rs10484358
rs10484358
1 1.000 0.040 6 16255812 intron variant G/T snv 7.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs10994338
rs10994338
3 0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs11773103
rs11773103
2 0.925 0.040 7 87192664 non coding transcript exon variant A/G snv 4.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs12054895
rs12054895
1 1.000 0.040 5 27611324 intergenic variant G/T snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs12410462
rs12410462
1 1.000 0.040 1 227480089 upstream gene variant G/A snv 0.12 0.800 1.000 1 2013 2013
dbSNP: rs12446956
rs12446956
1 1.000 0.040 16 73467637 intron variant T/C snv 9.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs12912251
rs12912251
3 0.882 0.080 15 38694167 intron variant G/T snv 0.25 0.800 1.000 1 2011 2011
dbSNP: rs17077540
rs17077540
1 1.000 0.040 18 67618042 intron variant A/G snv 0.10 0.800 1.000 1 2011 2011
dbSNP: rs17082664
rs17082664
2 0.925 0.040 6 152417619 intron variant A/G snv 0.17 0.800 1.000 1 2011 2011
dbSNP: rs17538444
rs17538444
1 1.000 0.040 13 43260134 intron variant C/T snv 5.1E-02 0.800 1.000 1 2013 2013
dbSNP: rs17651119
rs17651119
1 1.000 0.040 5 16812529 intron variant C/T snv 2.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs17692896
rs17692896
1 1.000 0.040 19 32598525 intron variant G/A snv 4.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs2546057
rs2546057
3 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 0.800 1.000 1 2013 2013
dbSNP: rs270545
rs270545
1 1.000 0.040 5 38051491 intron variant G/A snv 0.30 0.800 1.000 1 2011 2011
dbSNP: rs2828520
rs2828520
1 1.000 0.040 21 23770802 intergenic variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs4585146
rs4585146
1 1.000 0.040 3 192100853 intron variant G/A snv 0.30 0.800 1.000 1 2013 2013
dbSNP: rs6537837
rs6537837
1 1.000 0.040 1 109577110 intron variant C/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs6799788
rs6799788
1 1.000 0.040 3 159926508 intron variant A/G snv 0.18 0.800 1.000 1 2013 2013
dbSNP: rs7174755
rs7174755
1 1.000 0.040 15 68304789 intron variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs7713917
rs7713917
3 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 0.800 1.000 1 2010 2010
dbSNP: rs8050326
rs8050326
1 1.000 0.040 16 86070536 regulatory region variant G/A snv 0.49 0.800 1.000 1 2013 2013
dbSNP: rs139438618
rs139438618
5 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 0.710 1.000 1 2017 2017
dbSNP: rs2715157
rs2715157
1 1.000 0.040 7 82839058 intron variant A/G;T snv 0.710 1.000 1 2017 2017
dbSNP: rs10020288
rs10020288
2 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 0.700 1.000 1 2018 2018