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: rs10054105
rs10054105
3 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs11084596
rs11084596
3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11199879
rs11199879
3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11651052
rs11651052
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs148678804
rs148678804
2 1.000 0.040 10 22138360 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1638703
rs1638703
2 1.000 0.040 13 50514220 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs17144046
rs17144046
4 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs17779457
rs17779457
2 1.000 0.080 9 27488094 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs200383755
rs200383755
3 0.925 0.080 20 62475466 missense variant G/C snv 3.4E-03 3.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs200476
rs200476
2 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs2555019
rs2555019
3 1.000 0.040 12 114230813 intergenic variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2556378
rs2556378
3 1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs2853677
rs2853677
19 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs2981575
rs2981575
4 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs381949
rs381949
3 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs4548546
rs4548546
3 1.000 0.040 10 120870067 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6061244
rs6061244
2 1.000 0.040 20 62466597 intron variant G/A;C snv 1.3E-03; 0.38 0.700 1.000 1 2018 2018
dbSNP: rs6561599
rs6561599
2 1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs677394
rs677394
2 1.000 0.040 5 135271869 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs72878024
rs72878024
2 1.000 0.040 11 199492 missense variant G/A snv 6.4E-02 6.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs7906649
rs7906649
2 1.000 0.040 10 22021369 intergenic variant G/A snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs8853
rs8853
4 0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs9958656
rs9958656
2 1.000 0.040 18 22324181 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10903035
rs10903035
2 1.000 0.080 1 24155450 3 prime UTR variant G/A snv 0.63 0.010 1.000 1 2015 2015
dbSNP: rs12979860
rs12979860
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015