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: rs9465627
rs9465627
2 6 10233702 intergenic variant T/G snv 6.5E-03 0.700 1.000 1 2017 2017
dbSNP: rs145811080
rs145811080
2 10 124459913 upstream gene variant G/A snv 6.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs651007
rs651007
22 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs17415853
rs17415853
2 12 15777871 intron variant T/C snv 2.0E-02 0.700 1.000 1 2008 2008
dbSNP: rs191752533
rs191752533
2 7 16788068 downstream gene variant T/G snv 3.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs744653
rs744653
4 2 189514024 regulatory region variant C/T snv 0.84 0.700 1.000 1 2014 2014
dbSNP: rs5742933
rs5742933
5 0.882 0.080 2 189784590 5 prime UTR variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs5743077
rs5743077
2 2 189832613 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs987710
rs987710
4 1.000 0.040 22 22158022 intron variant G/A snv 0.61 0.700 1.000 1 2011 2011
dbSNP: rs17342717
rs17342717
8 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 2 2011 2011
dbSNP: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.700 1.000 1 2017 2017
dbSNP: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.700 1.000 2 2011 2014
dbSNP: rs76858924
rs76858924
2 6 26261299 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs760719
rs760719
2 22 37064409 downstream gene variant C/T snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs855791
rs855791
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.700 1.000 2 2014 2017
dbSNP: rs10064177
rs10064177
2 5 4439147 non coding transcript exon variant G/A snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs411988
rs411988
2 17 58631673 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs74450770
rs74450770
2 16 66237397 intergenic variant T/C snv 7.2E-03 0.700 1.000 1 2017 2017
dbSNP: rs217181
rs217181
6 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs9302635
rs9302635
4 16 72110275 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs113036595
rs113036595
2 13 95480065 intron variant T/- del 0.46 0.700 1.000 1 2017 2017