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: 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: 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: 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: 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: 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
dbSNP: rs1447352
rs1447352
2 11 92989595 downstream gene variant G/A snv 0.55 0.800 1.000 1 2009 2009
dbSNP: rs1495743
rs1495743
6 8 18415790 intergenic variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs17277546
rs17277546
4 7 99891948 3 prime UTR variant G/A snv 3.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs2023634
rs2023634
2 22 18984937 intron variant A/G snv 7.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs2066938
rs2066938
3 12 120722812 3 prime UTR variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2087160
rs2087160
2 4 110413574 intron variant G/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs211718
rs211718
3 1 75640990 downstream gene variant T/C snv 0.75 0.700 1.000 1 2011 2011
dbSNP: rs2216405
rs2216405
2 2 210752170 intergenic variant A/G snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs2232326
rs2232326
3 2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs2403254
rs2403254
2 11 18303599 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2411884
rs2411884
2 11 2714304 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2518049
rs2518049
2 10 5095844 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2624265
rs2624265
3 15 38856448 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009