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: rs2114835
rs2114835
1 10 124941988 intron variant C/T snv 0.82 0.700 1.000 1 2012 2012
dbSNP: rs8141529
rs8141529
1 22 28873704 intergenic variant A/G snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs259981
rs259981
1 20 59173314 intron variant T/A snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs13535
rs13535
1 19 9343497 3 prime UTR variant A/G snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs11784860
rs11784860
1 8 144788414 upstream gene variant C/T snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs9901737
rs9901737
1 17 32354335 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6438885
rs6438885
1 3 125241998 intron variant C/T snv 0.78 0.700 1.000 1 2012 2012
dbSNP: rs1060379
rs1060379
1 7 64975111 3 prime UTR variant A/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs149290349
rs149290349
3 2 43224818 missense variant G/A;T snv 6.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs7650602
rs7650602
2 1.000 0.040 3 141428572 intron variant T/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs17600797
rs17600797
1 4 44624789 splice region variant C/A;T snv 0.21; 1.6E-04 0.700 1.000 1 2012 2012
dbSNP: rs16937223
rs16937223
1 8 70772910 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1381817
rs1381817
1 2 19979459 intron variant C/T snv 7.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs17011715
rs17011715
1 10 49053732 intron variant T/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs10424282
rs10424282
1 19 49989603 intron variant C/G;T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs4802260
rs4802260
1 19 45524494 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8182269
rs8182269
1 17 78793909 intron variant A/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs6807974
rs6807974
2 1.000 0.040 3 179682158 intron variant A/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1556260
rs1556260
1 1 161044656 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10901450
rs10901450
1 10 125820725 intron variant G/C snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs11077815
rs11077815
1 17 76393809 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs5754100
rs5754100
5 0.882 22 21561877 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs6974485
rs6974485
1 7 67149319 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2847153
rs2847153
3 0.925 0.080 18 661647 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs7841518
rs7841518
1 8 33506102 intron variant G/C snv 0.64 0.700 1.000 1 2012 2012