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: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2011 2018
dbSNP: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2011 2016
dbSNP: rs10096633
rs10096633
8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs10244051
rs10244051
3 1.000 0.080 7 15024208 intergenic variant T/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs10518693
rs10518693
IVD
2 15 40407823 intron variant C/T snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs10799701
rs10799701
2 1 21494497 intergenic variant A/G snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs10885409
rs10885409
3 1.000 0.080 10 113048313 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs10965246
rs10965246
2 9 22132699 downstream gene variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs11185790
rs11185790
3 10 89612776 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs11705729
rs11705729
3 1.000 0.080 3 185789511 intron variant A/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs11924032
rs11924032
3 3 171017310 intron variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs1203936
rs1203936
2 20 22611792 upstream gene variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12053049
rs12053049
2 2 168910638 intron variant T/C snv 5.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs12310617
rs12310617
16 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179
16 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs12420422
rs12420422
16 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs12670403
rs12670403
2 7 17269655 intron variant C/A snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs12712928
rs12712928
2 2 44964941 intron variant G/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs12753193
rs12753193
3 1 65703996 non coding transcript exon variant G/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs13114738
rs13114738
16 0.851 0.120 4 102363708 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs13391552
rs13391552
2 2 73591809 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1349497
rs1349497
2 2 172727935 intron variant G/A;C snv 0.700 1.000 1 2018 2018