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: rs34290285
rs34290285
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs410867
rs410867
2 19 16316300 intron variant A/G snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs45577137
rs45577137
4 8 47739071 upstream gene variant A/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs4802399
rs4802399
2 19 38409359 3 prime UTR variant G/A snv 5.5E-02 0.700 1.000 2 2016 2019
dbSNP: rs4848100
rs4848100
2 2 111630955 non coding transcript exon variant C/T snv 0.76 0.700 1.000 2 2016 2019
dbSNP: rs511515
rs511515
2 6 33573730 3 prime UTR variant A/G snv 0.73 0.700 1.000 2 2016 2019
dbSNP: rs56330463
rs56330463
2 5 148820448 upstream gene variant T/C snv 0.59 0.700 1.000 2 2016 2019
dbSNP: rs61612642
rs61612642
2 6 42229969 intron variant C/T snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs62408225
rs62408225
2 1.000 0.120 6 90246690 intron variant A/G snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs6568466
rs6568466
2 6 107122949 intergenic variant T/C snv 0.58 0.700 1.000 2 2016 2019
dbSNP: rs6684992
rs6684992
2 1 87286317 intergenic variant A/T snv 0.20 0.700 1.000 2 2016 2018
dbSNP: rs6920211
rs6920211
4 6 135110180 regulatory region variant T/C snv 0.29 0.700 1.000 2 2016 2019
dbSNP: rs7288670
rs7288670
4 22 24225858 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs73072483
rs73072483
2 3 50734193 intron variant G/A snv 9.6E-02 0.700 1.000 2 2016 2019
dbSNP: rs74480102
rs74480102
3 17 7839283 upstream gene variant G/A snv 2.5E-02 0.700 1.000 2 2016 2019
dbSNP: rs7569084
rs7569084
2 2 65429835 intron variant C/T snv 0.62 0.700 1.000 2 2016 2019
dbSNP: rs8179
rs8179
8 0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs9504361
rs9504361
3 1.000 0.040 6 577820 intron variant A/G snv 0.40 0.700 1.000 2 2016 2019
dbSNP: rs960709
rs960709
5 0.882 0.120 5 151081488 intron variant A/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs9829778
rs9829778
2 3 196822218 intron variant G/A snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs9900933
rs9900933
UNK
3 17 75805073 intron variant T/A;C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs9979383
rs9979383
5 0.925 0.200 21 35343463 intron variant C/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs1000005
rs1000005
1 21 33060745 intron variant G/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10045577
rs10045577
1 5 111090753 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004870
rs1004870
1 1 41905116 intron variant C/T snv 0.57 0.700 1.000 1 2019 2019