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: rs1145652
rs1145652
1 5 165337081 intergenic variant A/G snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs11662721
rs11662721
1 18 21681452 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs11667159
rs11667159
3 19 46291989 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11668290
rs11668290
3 19 46292921 upstream gene variant G/A snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671319
rs11671319
3 19 46291810 intergenic variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671360
rs11671360
3 19 46291914 intergenic variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671710
rs11671710
3 19 46288677 regulatory region variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs116843064
rs116843064
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11730235
rs11730235
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs117366905
rs117366905
3 19 46294033 upstream gene variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs117992292
rs117992292
3 19 46294038 upstream gene variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12098564
rs12098564
2 10 85193571 non coding transcript exon variant A/G snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs12190237
rs12190237
1 6 10922405 intron variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587
1 6 10989709 synonymous variant G/A snv 0.12 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12213249
rs12213249
1 6 10926709 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs1225717
rs1225717
1 6 10978007 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1225736
rs1225736
1 6 10939156 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1225737
rs1225737
1 6 10982419 3 prime UTR variant C/T snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1225741
rs1225741
1 6 10952010 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs1225744
rs1225744
1 6 10954307 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs1225753
rs1225753
1 6 10956456 intron variant G/A snv 0.43 0.700 1.000 1 2011 2011