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: rs10811652
rs10811652
CDKN2B-AS1
4 0.882 0.120 9 22077086 intron variant A/C;T snv 0.710 1.000 1 2018 2018
dbSNP: rs12541758
rs12541758
LOC392232
2 0.925 0.080 8 72230147 non coding transcript exon variant C/T snv 0.34 0.710 1.000 1 2016 2016
dbSNP: rs139401390
rs139401390 		5 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 0.710 1.000 1 2019 2019
dbSNP: rs17165136
rs17165136
THSD7A
1 1.000 0.040 7 11739348 intron variant A/G snv 4.8E-02 0.710 1.000 1 2018 2018
dbSNP: rs7421388
rs7421388
PLCL1
2 0.925 0.080 2 198223806 intron variant A/C;G snv 0.710 1.000 1 2016 2016
dbSNP: rs74617384
rs74617384
LPA
5 0.925 0.080 6 160576086 intron variant A/G;T snv 0.710 1.000 1 2018 2018
dbSNP: rs852787
rs852787
DAB1
1 1.000 0.040 1 57836430 intron variant C/T snv 0.16 0.710 1.000 1 2018 2018
dbSNP: rs9486729
rs9486729
SCML4
1 1.000 0.040 6 107824597 upstream gene variant A/C;G snv 0.710 1.000 1 2018 2018
dbSNP: rs10093110
rs10093110
ZFPM2 ; ZFPM2-AS1 ; LOC105375696
1 1.000 0.040 8 105553186 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10106652
rs10106652 		3 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs10128951
rs10128951
SCARB1
1 1.000 0.040 12 124855901 intron variant G/A snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs10131519
rs10131519
EML1
1 1.000 0.040 14 99892957 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs10131894
rs10131894 		2 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs10186133
rs10186133 		1 1.000 0.040 2 113079367 downstream gene variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10221742
rs10221742 		1 1.000 0.040 2 21196778 downstream gene variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10237377
rs10237377
PARP12
1 1.000 0.040 7 140057336 intron variant G/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs10249651
rs10249651
CFTR ; ASZ1
1 1.000 0.040 7 117424571 intron variant T/C snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10267593
rs10267593
MAD1L1
1 1.000 0.040 7 1897625 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs1034246
rs1034246
PTK7
1 1.000 0.040 6 43100632 intron variant G/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10456100
rs10456100
KCNK5
2 1.000 0.040 6 39215694 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10495907
rs10495907 		1 1.000 0.040 2 43771587 upstream gene variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs1050362
rs1050362
DHX38
1 1.000 0.040 16 72096916 missense variant C/A;T snv 0.38; 2.4E-05 0.700 1.000 1 2018 2018
dbSNP: rs10512861
rs10512861
DNAJC13
1 1.000 0.040 3 132539117 downstream gene variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10734649
rs10734649
SBF2-AS1 ; LINC02709
1 1.000 0.040 11 9759344 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10757264
rs10757264
CDKN2B-AS1
2 1.000 0.040 9 22019733 intron variant A/G snv 0.58 0.700 1.000 1 2007 2007