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: rs6562760
rs6562760
1 1.000 0.080 13 73383544 intergenic variant A/G snv 0.76 0.700 1.000 3 2016 2017
dbSNP: rs1053338
rs1053338
1 1.000 0.080 3 63982224 missense variant A/G snv 0.14; 1.2E-05 0.10 0.700 1.000 2 2015 2017
dbSNP: rs11627032
rs11627032
1 1.000 0.080 14 92637727 intron variant T/C snv 0.22 0.700 1.000 2 2015 2017
dbSNP: rs12048493
rs12048493
1 1.000 0.080 1 149955122 intron variant A/C snv 0.29 0.700 1.000 2 2015 2017
dbSNP: rs12870942
rs12870942
1 1.000 0.080 13 73232845 intergenic variant T/C snv 0.23 0.700 1.000 2 2016 2017
dbSNP: rs13162653
rs13162653
1 1.000 0.080 5 16187419 downstream gene variant G/A;C;T snv 0.700 1.000 2 2015 2017
dbSNP: rs13365225
rs13365225
1 1.000 0.080 8 37000965 intergenic variant A/G snv 0.26 0.700 1.000 2 2015 2017
dbSNP: rs1744947
rs1744947
1 1.000 0.080 14 68214759 intron variant C/T snv 0.18 0.800 1.000 2 2012 2017
dbSNP: rs2012709
rs2012709
1 1.000 0.080 5 32567626 intron variant C/T snv 0.37 0.700 1.000 2 2015 2017
dbSNP: rs3215401
rs3215401
1 1.000 0.080 5 1296140 upstream gene variant -/G delins 0.25 0.700 1.000 2 2017 2017
dbSNP: rs6507583
rs6507583
1 1.000 0.080 18 44819625 intron variant A/G snv 0.15 0.700 1.000 2 2015 2017
dbSNP: rs66823261
rs66823261
1 1.000 0.080 8 220692 intron variant T/A;C snv 0.700 1.000 2 2017 2017
dbSNP: rs7707921
rs7707921
1 1.000 0.080 5 82242227 intron variant T/A snv 0.81 0.700 1.000 2 2015 2017
dbSNP: rs78540526
rs78540526
1 1.000 0.080 11 69516650 regulatory region variant C/T snv 5.2E-02 0.700 1.000 2 2015 2017
dbSNP: rs9257408
rs9257408
1 1.000 0.080 6 28958443 TF binding site variant G/A;C;T snv 0.700 1.000 2 2015 2017
dbSNP: rs10022462
rs10022462
1 1.000 0.080 4 88322666 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs10096351
rs10096351
1 1.000 0.080 8 127359926 intron variant A/G snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs10169133
rs10169133
1 1.000 0.080 2 19212878 intron variant G/C;T snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs10269006
rs10269006
1 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs1028842
rs1028842
1 1.000 0.080 14 68205006 intron variant C/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs10510097
rs10510097
1 1.000 0.080 10 121568362 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs10623258
rs10623258
1 1.000 0.080 14 104745924 non coding transcript exon variant -/TT ins 0.56 0.700 1.000 1 2017 2017
dbSNP: rs10629804
rs10629804
1 1.000 0.080 5 123142307 intron variant -/TTCAC delins 0.72 0.700 1.000 1 2017 2017
dbSNP: rs10644111
rs10644111
1 1.000 0.080 7 92022864 protein altering variant -/AAC delins 0.39 0.46 0.700 1.000 1 2017 2017
dbSNP: rs10760444
rs10760444
1 1.000 0.080 9 126634155 intron variant G/A snv 0.51 0.700 1.000 1 2017 2017