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: rs3743073
rs3743073
CHRNA3
11 0.807 0.120 15 78617197 intron variant G/T snv 0.61 0.010 1.000 1 2010 2010
dbSNP: rs3756824
rs3756824
PRL ; CASC15
3 0.925 0.080 6 22298508 intron variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs3774937
rs3774937
NFKB1
9 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.010 1.000 1 2019 2019
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: rs3804329
rs3804329
ATG5
2 1.000 0.080 6 106238552 intron variant A/G snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs3804639
rs3804639
CD47
1 3 108071988 intron variant G/T snv 0.28 0.010 1.000 1 2013 2013
dbSNP: rs3923594
rs3923594
MCAM
2 1.000 0.120 11 119317205 intron variant C/A;T snv 7.1E-06 0.010 1.000 1 2017 2017
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
7 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2013 2013
dbSNP: rs4461062
rs4461062
NUP93
2 1.000 0.080 16 56830706 intron variant C/T snv 0.48 0.48 0.010 1.000 1 2019 2019
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: rs477145
rs477145
TIAM1
4 1.000 0.120 21 31390097 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs4946728
rs4946728
ATG5
3 1.000 0.120 6 106142488 intron variant A/C snv 0.72 0.010 1.000 1 2014 2014
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: rs60745952
rs60745952
LOC105377481 ; LOC107986195
6 0.925 0.080 4 148827842 intron variant T/C snv 0.13 0.010 < 0.001 1 2016 2016
dbSNP: rs629367
rs629367
MIR100HG ; MIRLET7A2
11 0.776 0.200 11 122146306 intron variant C/A snv 0.88 0.010 1.000 1 2018 2018
dbSNP: rs6464926
rs6464926
EZH2
4 0.882 0.120 7 148821919 intron variant C/T snv 0.41 0.010 1.000 1 2018 2018
dbSNP: rs684559
rs684559
CHI3L2
1 1 111215824 intron variant G/A snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs6973569
rs6973569
NPSR1-AS1
5 0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs6983561
rs6983561
PCAT1 ; CASC19
3 0.925 0.080 8 127094635 intron variant A/C snv 0.17 0.010 1.000 1 2011 2011
dbSNP: rs723526
rs723526
EGFR
2 1.000 7 55067126 intron variant A/G snv 0.86 0.010 1.000 1 2013 2013
dbSNP: rs7371084
rs7371084
LHCGR ; GTF2A1L ; STON1-GTF2A1L
3 0.925 0.120 2 48712814 intron variant T/C snv 0.12 0.010 1.000 1 2012 2012
dbSNP: rs7646409
rs7646409
PIK3CA
4 0.882 0.040 3 179182405 intron variant T/C snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs7668666
rs7668666
TLR3
4 1.000 4 186080138 intron variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs767649
rs767649
MIR155HG ; MIR155
18 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 0.010 1.000 1 2015 2015
dbSNP: rs7758229
rs7758229
SLC22A3
16 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2017 2017