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: rs994308
rs994308 		10 0.776 0.080 20 6622975 intergenic variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs9939049
rs9939049
CDH1
9 0.790 0.080 16 68778398 intron variant A/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs9930005
rs9930005 		10 0.776 0.080 16 80009361 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9929218
rs9929218
CDH1
16 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
dbSNP: rs9924886
rs9924886
CDH3
10 0.776 0.080 16 68710036 intron variant A/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs992157
rs992157
PNKD ; TMBIM1
10 0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 0.700 1.000 2 2018 2019
dbSNP: rs9901225
rs9901225
RETREG3
10 0.790 0.080 17 42603793 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs9834244
rs9834244 		10 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs983402
rs983402 		10 0.776 0.080 2 198916862 intron variant T/C snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs983318
rs983318
LINC00511 ; LINC00673
10 0.776 0.080 17 72417112 intron variant G/A snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs9831861
rs9831861 		9 0.790 0.080 3 53054269 intron variant T/G snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs9797885
rs9797885
TMEM91
9 0.790 0.080 19 41367096 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9733843
rs9733843 		9 0.790 0.080 10 8676041 intergenic variant A/G snv 0.24 0.700 1.000 1 2018 2018
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: rs961253
rs961253 		15 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 0.700 1.000 4 2008 2019
dbSNP: rs9583269
rs9583269
MYO16
9 0.790 0.080 13 108630682 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs9537521
rs9537521
STARD13
9 0.790 0.080 13 33464043 intron variant G/A snv 0.20 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: rs9481067
rs9481067
SLC22A16
10 0.776 0.080 6 110429349 intron variant A/G snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9409565
rs9409565
LOC107987100
9 0.790 0.080 9 94488752 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9271770
rs9271770 		10 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs9271695
rs9271695 		10 0.776 0.080 6 32625303 upstream gene variant A/G snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs899244
rs899244 		9 0.790 0.080 16 86666424 intron variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs847208
rs847208 		9 0.790 0.080 16 86220445 downstream gene variant C/A snv 0.70 0.700 1.000 2 2018 2019