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: rs12594720
rs12594720
10 0.776 0.080 15 66714680 intron variant C/G snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12672022
rs12672022
10 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs12708491
rs12708491
10 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13086367
rs13086367
10 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs13149359
rs13149359
10 0.776 0.080 4 94017467 intergenic variant C/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs13204733
rs13204733
10 0.776 0.080 6 55701310 intergenic variant A/G snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
11 0.763 0.240 4 105207603 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs1427760
rs1427760
10 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs145364999
rs145364999
10 0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs1537372
rs1537372
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs16878812
rs16878812
10 0.776 0.080 6 35601785 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs16969681
rs16969681
10 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs17011141
rs17011141
10 0.776 0.080 1 221939292 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs17094983
rs17094983
10 0.776 0.080 14 58722643 intron variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs1741640
rs1741640
10 0.776 0.080 20 62357358 intron variant T/C snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs174533
rs174533
18 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 0.700 1.000 1 2019 2019
dbSNP: rs17816465
rs17816465
10 0.776 0.080 15 32864185 intron variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs189583
rs189583
10 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1924816
rs1924816
10 0.776 0.080 13 73423824 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1963413
rs1963413
10 0.776 0.080 19 41365668 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2186607
rs2186607
10 0.776 0.080 11 101785666 intron variant T/A snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs2250430
rs2250430
10 0.776 0.080 12 6312008 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2293581
rs2293581
10 0.776 0.080 15 32718535 5 prime UTR variant G/A;C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs2516420
rs2516420
10 0.776 0.080 6 31481843 intron variant C/T snv 7.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs2735940
rs2735940
25 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 0.700 1.000 1 2019 2019