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: rs159963
rs159963
3 1.000 0.040 1 8444361 intron variant C/A snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs16917546
rs16917546
6 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs1695315
rs1695315
1 3 3111655 intron variant G/A snv 0.56 0.700 1.000 2 2016 2019
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs175705
rs175705
2 14 75509305 intergenic variant C/A;G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
10 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
dbSNP: rs2075995
rs2075995
3 1 23520972 missense variant C/A snv 0.45 0.39 0.700 1.000 2 2016 2019
dbSNP: rs2228467
rs2228467
8 1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 0.700 1.000 2 2016 2019
dbSNP: rs2239633
rs2239633
12 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 0.700 1.000 2 2016 2019
dbSNP: rs2296618
rs2296618
2 1 198697103 intron variant A/G snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs2579500
rs2579500
1 2 96535945 upstream gene variant G/A;C snv 0.700 1.000 2 2016 2019
dbSNP: rs2960422
rs2960422
2 1.000 0.080 3 12293492 intron variant G/A snv 0.59 0.700 1.000 2 2016 2019
dbSNP: rs34173062
rs34173062
3 8 144103704 missense variant G/A;C snv 7.3E-02 0.700 1.000 2 2016 2019
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: rs36084354
rs36084354
3 19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 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: rs61731111
rs61731111
2 19 3179519 missense variant C/G;T snv 1.3E-02 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