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: rs200820567
rs200820567 		4 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 0.010 1.000 1 2017 2017
dbSNP: rs2132039
rs2132039
UGT2B28
2 0.925 0.120 4 69293669 intron variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs2280714
rs2280714
TNPO3
10 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 0.010 1.000 1 2018 2018
dbSNP: rs2596542
rs2596542
MICA ; MICA-AS1
18 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 0.010 1.000 1 2013 2013
dbSNP: rs2617160
rs2617160
KLRC4-KLRK1 ; LOC101928100
1 1.000 0.080 12 10392998 intron variant A/C;T snv 0.010 1.000 1 2010 2010
dbSNP: rs2794521
rs2794521
CRP
15 0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 0.010 1.000 1 2019 2019
dbSNP: rs2853953
rs2853953 		1 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs3024490
rs3024490
IL10 ; IL19
11 0.742 0.520 1 206771966 intron variant A/C;G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs3106796
rs3106796
COL3A1 ; LOC105373791
3 0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 0.010 1.000 1 2008 2008
dbSNP: rs3130542
rs3130542 		8 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 0.700 1.000 1 2015 2015
dbSNP: rs35761398
rs35761398
CNR2
19 0.701 0.520 1 23875429 missense variant TT/CC mnv 0.010 1.000 1 2015 2015
dbSNP: rs3759333
rs3759333
LTBR
3 0.882 0.120 12 6382781 intron variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs3806798
rs3806798
IL15
2 0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 0.010 1.000 1 2014 2014
dbSNP: rs4845384
rs4845384
ADAR
1 1.000 0.080 1 154615193 intron variant A/G snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs4935047
rs4935047
MBL2
1 1.000 0.080 10 52770307 intron variant A/G snv 0.49 0.010 < 0.001 1 2013 2013
dbSNP: rs510432
rs510432
ATG5
11 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs61330082
rs61330082
NAMPT
13 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 0.010 1.000 1 2016 2016
dbSNP: rs61886277
rs61886277
PLCE1
1 1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs6715787
rs6715787
EPAS1
4 0.851 0.200 2 46349033 intron variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs705382
rs705382
PON1
5 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 0.010 1.000 1 2015 2015
dbSNP: rs7095891
rs7095891
MBL2
3 0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 0.010 < 0.001 1 2013 2013
dbSNP: rs7549785
rs7549785
FCER1A
3 0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 0.710 1.000 1 2019 2019
dbSNP: rs7712322
rs7712322
POLR3G
1 1.000 0.080 5 90482078 intron variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs7756516
rs7756516
HLA-DQB2
4 0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 0.700 1.000 1 2014 2014
dbSNP: rs78900671
rs78900671
COL22A1
1 1.000 0.080 8 138653967 intron variant G/A;C snv 0.700 1.000 1 2019 2019