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: rs1416742
rs1416742
1 1.000 0.120 9 16856885 intron variant G/A snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs185229225
rs185229225
4 0.851 0.120 4 13607505 intron variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs2153271
rs2153271
3 0.925 0.160 9 16864523 intron variant C/T snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs34289250
rs34289250
2 0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs367899983
rs367899983
2 1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 0.700 1.000 1 2009 2009
dbSNP: rs4445329
rs4445329
1 1.000 0.120 9 16911759 intergenic variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs4961501
rs4961501
1 1.000 0.120 9 16851680 intron variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs757210
rs757210
6 0.807 0.160 17 37736525 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7651446
rs7651446
3 0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs7861573
rs7861573
1 1.000 0.120 9 16862282 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs8170
rs8170
13 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1064795649
rs1064795649
2 1.000 0.120 17 61799205 frameshift variant CT/- delins 0.700 0
dbSNP: rs113954997
rs113954997
3 0.882 0.280 11 14294844 missense variant T/A;C snv 0.700 0
dbSNP: rs118203998
rs118203998
11 0.790 0.400 16 23603471 stop gained G/C;T snv 1.6E-05; 4.0E-06 0.700 0
dbSNP: rs1199923024
rs1199923024
1 1.000 0.120 17 61683945 missense variant G/A snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs121913286
rs121913286
23 0.677 0.280 3 179218306 missense variant C/A;G snv 0.700 0
dbSNP: rs121913322
rs121913322
4 0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 0.700 0
dbSNP: rs121913340
rs121913340
1 1.000 0.120 7 140753379 missense variant C/T snv 0.700 0
dbSNP: rs121913413
rs121913413
11 0.763 0.240 3 41224634 missense variant C/A;T snv 0.700 0
dbSNP: rs121964872
rs121964872
3 0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 0.700 0
dbSNP: rs137852986
rs137852986
13 0.732 0.440 17 61716051 stop gained G/A snv 1.7E-04 1.5E-04 0.700 0
dbSNP: rs138213197
rs138213197
24 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
dbSNP: rs1800726
rs1800726
1 1.000 0.120 17 43070993 missense variant C/G;T snv 0.700 0
dbSNP: rs1800751
rs1800751
5 0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs1800757
rs1800757
1 1.000 0.120 17 43051069 missense variant G/A snv 0.700 0