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: rs17249754
rs17249754
12 0.882 0.120 12 89666809 intron variant G/A snv 0.15 0.700 1.000 4 2011 2018
dbSNP: rs10184428
rs10184428
5 2 164155317 intron variant C/A;G snv 0.700 1.000 3 2018 2018
dbSNP: rs11191593
rs11191593
4 10 103179458 intron variant T/C snv 9.0E-02 0.700 1.000 3 2011 2018
dbSNP: rs1173771
rs1173771
9 5 32814922 regulatory region variant A/G snv 0.65 0.700 1.000 3 2011 2018
dbSNP: rs13107325
rs13107325
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 3 2011 2018
dbSNP: rs1458038
rs1458038
10 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 0.700 1.000 3 2011 2018
dbSNP: rs16998073
rs16998073
10 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 0.700 1.000 3 2016 2018
dbSNP: rs35443
rs35443
5 12 115115073 intergenic variant G/C snv 0.40 0.700 1.000 3 2018 2018
dbSNP: rs4980389
rs4980389
5 11 1871355 5 prime UTR variant G/A snv 0.35 0.700 1.000 3 2018 2018
dbSNP: rs604723
rs604723
9 1.000 0.040 11 100739815 intron variant T/C snv 0.78 0.700 1.000 3 2015 2018
dbSNP: rs633185
rs633185
10 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs880315
rs880315
9 0.925 0.120 1 10736809 intron variant T/C snv 0.32 0.700 1.000 3 2016 2018
dbSNP: rs1004467
rs1004467
13 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 0.700 1.000 2 2016 2018
dbSNP: rs10857147
rs10857147
9 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 0.700 1.000 2 2018 2018
dbSNP: rs1105956
rs1105956
2 6 126825734 intron variant G/A snv 0.44 0.700 1.000 2 2018 2018
dbSNP: rs111478946
rs111478946
4 12 89665065 intron variant G/A snv 0.14 0.700 1.000 2 2018 2018
dbSNP: rs11191871
rs11191871
2 10 103947673 intergenic variant A/G snv 5.2E-02 0.700 1.000 2 2018 2018
dbSNP: rs112913898
rs112913898
3 10 103199143 intergenic variant G/A snv 9.1E-02 0.700 1.000 2 2018 2018
dbSNP: rs1177765
rs1177765
3 5 32829823 intergenic variant T/C snv 0.50 0.700 1.000 2 2018 2018
dbSNP: rs12579302
rs12579302
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 2 2017 2018
dbSNP: rs1275988
rs1275988
6 1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 0.700 1.000 2 2015 2018
dbSNP: rs13139571
rs13139571
9 1.000 0.040 4 155724361 intron variant C/A snv 0.22 0.700 1.000 2 2011 2018
dbSNP: rs13149993
rs13149993
6 4 80237391 regulatory region variant G/A;C snv 0.700 1.000 2 2015 2018
dbSNP: rs1327235
rs1327235
7 20 10988382 intron variant A/G snv 0.46 0.700 1.000 2 2011 2018
dbSNP: rs1401982
rs1401982
4 12 89595822 intron variant G/A snv 0.60 0.700 1.000 2 2018 2018