Source: ALL
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: rs1001179
rs1001179
CAT
33 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs10155912
rs10155912
1 1.000 0.040 7 140058921 intron variant A/C snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs10200159
rs10200159
1 1.000 0.040 2 55617974 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10249788
rs10249788
6 0.827 0.160 7 17298523 intron variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs10250629
rs10250629
1 1.000 0.040 7 50151757 intron variant T/C snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs1031034
rs1031034
1 1.000 0.040 4 101302229 intron variant C/A snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs1041981
rs1041981
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.010 1.000 1 2013 2013
dbSNP: rs1043101
rs1043101
1 1.000 0.040 11 35253282 3 prime UTR variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10431924
rs10431924
3 0.882 0.120 16 68805399 intron variant T/C snv 0.45 0.010 1.000 1 2015 2015
dbSNP: rs1043210477
rs1043210477
19 0.701 0.520 3 49358250 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs10484554
rs10484554
11 0.807 0.200 6 31306778 intron variant C/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs10503019
rs10503019
2 0.925 0.040 18 57787145 intron variant G/A snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs10768122
rs10768122
1 1.000 0.040 11 35259305 3 prime UTR variant A/G snv 0.33 0.800 1.000 1 2012 2012
dbSNP: rs10774624
rs10774624
6 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs1079541
rs1079541
1 1.000 0.040 6 30438979 intergenic variant C/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs10876864
rs10876864
5 0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 0.810 1.000 1 2013 2013
dbSNP: rs10986311
rs10986311
1 1.000 0.040 9 124309214 intron variant T/C snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs11021232
rs11021232
1 1.000 0.040 11 95587644 intron variant T/C snv 0.14 0.800 1.000 2 2012 2016
dbSNP: rs11079035
rs11079035
3 1.000 0.040 17 42136994 intron variant G/A snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs11203203
rs11203203
9 0.807 0.240 21 42416077 intron variant G/A snv 0.28 0.800 1.000 2 2010 2012
dbSNP: rs1126809
rs1126809
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.700 1.000 1 2016 2016
dbSNP: rs1129038
rs1129038
8 0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 0.800 1.000 1 2012 2012
dbSNP: rs1130409
rs1130409
72 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 0.010 1.000 1 2013 2013
dbSNP: rs1135216
rs1135216
6 0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 0.020 0.500 2 2014 2017
dbSNP: rs1136410
rs1136410
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2013 2013