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: rs686288
rs686288
1 12 100982873 intron variant A/G snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs12803802
rs12803802
1 11 107800953 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs11067592
rs11067592
2 12 109631385 intergenic variant G/T snv 1.2E-03 0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
7 1 109928142 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs118107800
rs118107800
1 10 110871498 non coding transcript exon variant T/C snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs76053346
rs76053346
1 10 110996333 intron variant G/T snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs79105258
rs79105258
24 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs596406
rs596406
1 10 11182702 intron variant T/C snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs12231737
rs12231737
5 0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs11066280
rs11066280
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs7043196
rs7043196
1 9 114371911 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs13077101
rs13077101
4 3 120706484 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs12580745
rs12580745
1 12 129167622 intron variant T/C snv 3.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs10198552
rs10198552
2 2 134842306 intron variant T/C snv 6.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs9389268
rs9389268
6 1.000 0.080 6 135098493 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs17835714
rs17835714
1 6 136024992 intron variant C/T snv 3.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs73154660
rs73154660
1 3 157229738 intron variant A/G snv 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs2241339
rs2241339
3 2 169013785 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs144430312
rs144430312
1 10 17693720 intron variant T/C snv 3.4E-04 0.700 1.000 1 2018 2018
dbSNP: rs2477664
rs2477664
1 10 17833817 synonymous variant T/A snv 4.5E-04 0.49 0.700 1.000 1 2010 2010
dbSNP: rs10827785
rs10827785
1 10 17933413 intergenic variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs6855088
rs6855088
2 4 181783398 intergenic variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs2489201
rs2489201
1 10 18221519 intron variant G/A snv 0.62 0.700 1.000 1 2018 2018