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: rs1047964
rs1047964
3 11 117286177 3 prime UTR variant G/A;C;T snv 0.710 1.000 1 2011 2011
dbSNP: rs1406961
rs1406961
2 20 63264568 intron variant A/C snv 0.87 0.710 1.000 1 2011 2011
dbSNP: rs2143678
rs2143678
2 6 41655295 downstream gene variant G/T snv 0.19 0.710 1.000 1 2011 2011
dbSNP: rs4975709
rs4975709
2 5 1877166 downstream gene variant A/C;T snv 0.710 1.000 1 2011 2011
dbSNP: rs7698623
rs7698623
2 4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 0.710 1.000 1 2011 2011
dbSNP: rs10042590
rs10042590
1 5 88477501 intron variant G/A snv 5.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10059884
rs10059884
5 5 32832368 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1009358
rs1009358
2 1.000 0.080 2 65049318 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10107066
rs10107066
1 8 26542619 intron variant G/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10224210
rs10224210
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1030431
rs1030431
3 8 58399138 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10409243
rs10409243
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1044486
rs1044486
1 17 78796097 3 prime UTR variant G/A snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1048070
rs1048070
1 9 14735055 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10500326
rs10500326
1 16 4868325 intron variant G/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10740995
rs10740995
1 10 18156159 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1074703
rs1074703
1 8 101803258 intron variant C/A snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs10748798
rs10748798
1 10 100794914 intron variant C/T snv 0.91 0.700 1.000 1 2019 2019
dbSNP: rs10769254
rs10769254
4 11 47340914 intron variant G/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10786156
rs10786156
2 10 94254865 intron variant C/G snv 0.44 0.47 0.700 1.000 1 2019 2019
dbSNP: rs10816914
rs10816914
1 9 109998608 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10821967
rs10821967
1 10 62182180 downstream gene variant A/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs10824134
rs10824134
ADK
1 10 74261866 intron variant T/C snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs10832571
rs10832571
1 11 16239678 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs10849891
rs10849891
1 12 121473799 intron variant T/A;G snv 0.700 1.000 1 2019 2019