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: rs4954585
rs4954585 		9 0.790 0.080 2 136240824 intergenic variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4968127
rs4968127
NXN
10 0.776 0.080 17 906403 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs57046232
rs57046232 		9 0.790 0.080 20 6399697 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs58791712
rs58791712 		9 0.790 0.080 5 40281696 intergenic variant T/-;TT;TTT delins 0.700 1.000 1 2019 2019
dbSNP: rs6055286
rs6055286 		9 0.790 0.080 20 7737398 intergenic variant A/G;T snv 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: rs61389091
rs61389091
CHRDL2
10 0.776 0.080 11 74716876 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs61510274
rs61510274
SLCO2A1
9 0.790 0.080 3 134030671 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs6678517
rs6678517
LAMC1
10 0.776 0.080 1 183033504 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6928864
rs6928864 		9 0.790 0.080 6 105519019 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs694339
rs694339
CBLN2
9 0.790 0.080 18 72554745 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7121958
rs7121958
POLD3
10 0.776 0.080 11 74568967 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7315438
rs7315438
LOC105370003
9 0.790 0.080 12 115453598 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7528276
rs7528276
MACF1
9 0.790 0.080 1 39344315 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs7606562
rs7606562
PPP1R21
9 0.790 0.080 2 48459556 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7708610
rs7708610 		10 0.776 0.080 5 40102341 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7758229
rs7758229
SLC22A3
16 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7894531
rs7894531 		9 0.790 0.080 10 8692798 intergenic 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: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T 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: rs9797885
rs9797885
TMEM91
9 0.790 0.080 19 41367096 intron variant A/G;T snv 0.700 1.000 1 2019 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: rs9930005
rs9930005 		10 0.776 0.080 16 80009361 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1057519945
rs1057519945
POLE
12 0.776 0.200 12 132673703 missense variant C/A;T snv 0.700 0