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: rs110419
rs110419
8 0.827 0.200 11 8231306 intron variant A/G snv 0.42 0.850 1.000 7 2011 2020
dbSNP: rs6939340
rs6939340
4 0.851 0.160 6 22139775 intron variant A/G snv 0.62 0.840 1.000 4 2008 2017
dbSNP: rs4712653
rs4712653
3 0.882 0.080 6 22125735 intron variant T/C;G snv 0.830 1.000 6 2008 2017
dbSNP: rs9295536
rs9295536
3 0.882 0.080 6 22131700 intron variant C/A snv 0.58 0.830 1.000 5 2008 2017
dbSNP: rs6435862
rs6435862
5 0.827 0.160 2 214807822 intron variant G/A;C;T snv 0.830 1.000 4 2009 2019
dbSNP: rs3768716
rs3768716
4 0.851 0.080 2 214771070 intron variant T/C snv 0.16 0.820 1.000 4 2009 2019
dbSNP: rs17487792
rs17487792
3 0.882 0.080 2 214778776 intron variant C/T snv 0.16 0.810 1.000 3 2009 2019
dbSNP: rs11037575
rs11037575
4 0.882 0.080 11 43706780 intron variant T/C snv 0.36 0.810 1.000 2 2012 2017
dbSNP: rs17065417
rs17065417
3 0.882 0.080 6 104958399 intron variant A/C snv 0.10 0.810 1.000 2 2012 2017
dbSNP: rs7587476
rs7587476
1 1.000 0.040 2 214789163 intron variant T/A;C snv 0.800 1.000 2 2009 2012
dbSNP: rs4336470
rs4336470
1 1.000 0.040 6 104732910 intron variant C/T snv 0.45 0.800 1.000 1 2012 2012
dbSNP: rs2168101
rs2168101
7 0.827 0.200 11 8233861 intron variant C/A snv 0.24 0.730 1.000 4 2017 2020
dbSNP: rs6441201
rs6441201
3 0.882 0.080 3 158460535 intron variant G/A snv 0.51 0.720 1.000 2 2017 2018
dbSNP: rs35850753
rs35850753
8 0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 0.710 1.000 2 2014 2017
dbSNP: rs3796727
rs3796727
3 0.882 0.080 4 8611299 intron variant G/A snv 0.26 0.32 0.710 1.000 2 2017 2018
dbSNP: rs10895322
rs10895322
4 0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 0.710 1.000 1 2017 2017
dbSNP: rs10131293
rs10131293
1 1.000 0.040 14 22461166 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10132733
rs10132733
1 1.000 0.040 14 22477241 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10142552
rs10142552
1 1.000 0.040 14 22395232 intron variant G/A snv 3.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10148895
rs10148895
1 1.000 0.040 14 22254840 intron variant C/T snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs10155916
rs10155916
1 1.000 0.040 7 38286177 intergenic variant G/A snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs10162417
rs10162417
1 1.000 0.040 14 22460708 intron variant T/G snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs1040303
rs1040303
1 1.000 0.040 14 22403377 intron variant G/A snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10441090
rs10441090
1 1.000 0.040 7 38295217 upstream gene variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10483273
rs10483273
1 1.000 0.040 14 22448054 intron variant A/G snv 9.5E-02 0.700 1.000 1 2009 2009