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: rs35883536
rs35883536
2 1 100640978 non coding transcript exon variant G/A snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs4807440
rs4807440
3 19 1026478 upstream gene variant G/T snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs562752749
rs562752749
2 10 102805443 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTT;TTTTTTTTTTTT delins 0.700 1.000 1 2016 2016
dbSNP: rs12898000
rs12898000
2 14 103368791 upstream gene variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs8022179
rs8022179
2 14 103380950 upstream gene variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs7298732
rs7298732
2 12 10458392 upstream gene variant T/C snv 9.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs199741557
rs199741557
2 4 104943373 intron variant TC/- delins 2.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs605783
rs605783
2 6 10526140 intron variant T/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs9480737
rs9480737
2 6 107121073 intergenic variant A/G snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs12312487
rs12312487
2 12 108327859 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs150861794
rs150861794
2 13 108351457 intron variant C/T snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs75900305
rs75900305
2 13 109159737 intron variant -/C delins 0.25 0.700 1.000 1 2016 2016
dbSNP: rs1887639
rs1887639
2 13 109374581 intergenic variant T/C snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs17608459
rs17608459
2 1 109892706 upstream gene variant G/A snv 7.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs333947
rs333947
7 1 109928142 intron variant G/A snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs58814158
rs58814158
2 13 110167908 intron variant T/G snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs2062225
rs2062225
2 2 110993295 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs150449635
rs150449635
2 2 110994574 intron variant T/C snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs3789088
rs3789088
2 2 111033227 intron variant G/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs3789087
rs3789087
2 2 111034076 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs7578982
rs7578982
4 2 111078961 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs10980797
rs10980797
3 9 111150273 intron variant A/G;T snv 0.700 1.000 2 2016 2018
dbSNP: rs6734942
rs6734942
2 2 111153117 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10980800
rs10980800
3 9 111153625 intron variant T/C snv 0.21 0.700 1.000 3 2011 2017
dbSNP: rs12346772
rs12346772
2 9 111158319 intron variant A/G snv 0.18 0.700 1.000 1 2014 2014