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: rs1902341
rs1902341
1 3 31754078 intron variant C/T snv 0.49 0.810 1.000 1 2010 2010
dbSNP: rs653178
rs653178
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.800 1.000 1 2014 2014
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.710 1.000 2 2019 2020
dbSNP: rs755249
rs755249
5 1 39529402 3 prime UTR variant C/A;T snv 0.710 1.000 1 2016 2016
dbSNP: rs9584669
rs9584669
1 13 97711228 intergenic variant T/C snv 0.19 0.710 1.000 1 2015 2015
dbSNP: rs10046574
rs10046574
1 7 135485722 intron variant C/T snv 7.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs10428206
rs10428206
1 3 74485377 intron variant T/C snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs10467515
rs10467515
1 13 52927172 regulatory region variant A/G snv 1.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs10484876
rs10484876
1 6 52389351 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10851907
rs10851907
4 1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10979314
rs10979314
1 9 108310149 intergenic variant G/A snv 7.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs11039100
rs11039100
2 11 5805773 intron variant T/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs11066301
rs11066301
12 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11077983
rs11077983
1 17 82227312 upstream gene variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11190074
rs11190074
1 10 99361961 intron variant A/G snv 8.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs11206019
rs11206019
1 1 52794278 intron variant G/T snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs11220138
rs11220138
1 11 125585927 intron variant C/T snv 7.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs11466653
rs11466653
3 1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs11512640
rs11512640
1 11 125556427 intron variant G/T snv 7.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs118039278
rs118039278
LPA
2 6 160564494 intron variant G/A snv 4.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs11819158
rs11819158
1 10 99418299 intron variant G/T snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs11942139
rs11942139
1 4 6429357 intron variant T/C snv 2.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs12257301
rs12257301
1 10 86655778 intron variant G/A snv 7.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs12335314
rs12335314
1 8 124550784 intron variant T/G snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs12445943
rs12445943
1 16 78775175 intron variant G/A snv 0.17 0.700 1.000 1 2016 2016