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: rs57046232
rs57046232 		9 0.790 0.080 20 6399697 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs6031311
rs6031311
TOX2
10 0.776 0.080 20 44037835 intron variant C/T snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs6051080
rs6051080
FAM182A
10 0.790 0.080 20 25995038 intron variant A/G snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs6055286
rs6055286 		9 0.790 0.080 20 7737398 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6058093
rs6058093
PIGU
12 0.776 0.080 20 34625392 intron variant A/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs6061231
rs6061231 		9 0.790 0.080 20 62381861 downstream gene variant C/A snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs6063514
rs6063514 		11 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs6067417
rs6067417
LOC105372657
10 0.776 0.080 20 50367160 intergenic variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs6085661
rs6085661 		9 0.790 0.080 20 6712481 TF binding site variant C/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs6091189
rs6091189
RIPOR3
10 0.776 0.080 20 50639748 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs6091213
rs6091213 		9 0.790 0.080 20 50768208 TF binding site variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs964293
rs964293 		9 0.790 0.080 20 54200178 TF binding site variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs994308
rs994308 		10 0.776 0.080 20 6622975 intergenic variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs952665081
rs952665081
PAK5 ; LOC105372523
1 1.000 0.080 20 9580201 missense variant A/G snv 0.700 0
dbSNP: rs10411210
rs10411210
RHPN2
13 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
dbSNP: rs1800469
rs1800469
TGFB1 ; B9D2
78 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
dbSNP: rs11085466
rs11085466
LOC101929007
10 0.790 0.080 19 21569009 intron variant G/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs12979278
rs12979278
MAMSTR
9 0.790 0.080 19 48715345 synonymous variant C/T snv 0.46 0.40 0.700 1.000 1 2019 2019
dbSNP: rs13343954
rs13343954
RHPN2
9 0.790 0.080 19 33036982 intron variant T/C snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs1963413
rs1963413
B9D2 ; TMEM91
10 0.776 0.080 19 41365668 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs285245
rs285245 		9 0.790 0.080 19 16310006 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs28541881
rs28541881
KIAA0355
9 0.790 0.080 19 34277685 intron variant C/T snv 9.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs28840750
rs28840750
RHPN2
10 0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs34797592
rs34797592 		10 0.776 0.080 19 16306387 intron variant C/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs4808075
rs4808075
BABAM1 ; USHBP1
18 0.701 0.280 19 17279482 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016