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: rs2622621
rs2622621
ABCG2
6 0.851 0.240 4 88109768 intron variant C/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2881766
rs2881766
ESR1
5 0.882 0.120 6 151797984 intron variant T/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs290481
rs290481
TCF7L2
9 0.827 0.200 10 113164066 intron variant C/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs3020449
rs3020449
ESR2
10 0.807 0.200 14 64306674 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs3218038
rs3218038
CCNE1
4 0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02 0.010 1.000 1 2012 2012
dbSNP: rs34214448
rs34214448
NME1 ; NME1-NME2
7 0.851 0.120 17 51154651 intron variant G/T snv 0.39 0.010 1.000 1 2012 2012
dbSNP: rs34904192
rs34904192
MIR155HG
1 1.000 0.080 21 25569623 intron variant G/A snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs3748093
rs3748093
BRAF
4 0.925 0.120 7 140800651 intron variant T/A snv 1.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs3790843
rs3790843
NR5A2
7 0.827 0.160 1 200041696 intron variant C/T snv 0.29 0.010 1.000 1 2014 2014
dbSNP: rs3801004
rs3801004
FSCN1
3 0.882 0.120 7 5598591 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs3917356
rs3917356
IL1B
4 0.882 0.160 2 112834786 intron variant C/T snv 0.39 0.010 1.000 1 2012 2012
dbSNP: rs42490
rs42490
RIPK2
5 0.882 0.160 8 89766285 intron variant G/A snv 0.60 0.010 1.000 1 2012 2012
dbSNP: rs4671393
rs4671393
BCL11A
11 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs4693608
rs4693608
HPSE
6 0.827 0.200 4 83320204 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs4784227
rs4784227
CASC16
8 0.807 0.160 16 52565276 intron variant C/T snv 0.20 0.010 1.000 1 2020 2020
dbSNP: rs4938723
rs4938723
BTG4 ; MIR34B ; MIR34C ; LOC728196
60 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
dbSNP: rs514049
rs514049
ADAM10
6 0.827 0.160 15 58750164 intron variant C/A snv 0.57 0.010 1.000 1 2018 2018
dbSNP: rs6720283
rs6720283
COL6A3
4 0.882 0.120 2 237401239 intron variant G/A snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs7166348
rs7166348
IGF1R
2 1.000 0.080 15 98704566 intron variant G/A;T snv 0.21 0.010 1.000 1 2016 2016
dbSNP: rs7186053
rs7186053
CDH1
1 1.000 0.080 16 68805390 intron variant A/G snv 0.69 0.010 1.000 1 2015 2015
dbSNP: rs738722
rs738722
CHEK2
4 0.882 0.120 22 28734024 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
dbSNP: rs8105637
rs8105637
TINCR
2 0.925 0.120 19 5566221 intron variant A/G snv 0.56 0.010 1.000 1 2017 2017
dbSNP: rs9679162
rs9679162
GALNT14
4 0.882 0.120 2 31024648 intron variant G/T snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs17530068
rs17530068
LOC105377871
3 0.882 0.120 6 81483392 intergenic variant T/C snv 0.19 0.010 1.000 1 2020 2020
dbSNP: rs116909374
rs116909374 		11 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 0.010 1.000 1 2019 2019