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: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.010 1.000 1 2015 2015
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2018 2018
dbSNP: rs182455
rs182455
STMN1 ; LOC105376885
2 0.925 0.120 1 25908492 upstream gene variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2271933
rs2271933
HCRTR1
9 0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 0.010 1.000 1 2019 2019
dbSNP: rs2295633
rs2295633
FAAH
7 0.827 0.120 1 46408711 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs2794520
rs2794520 		9 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs3100127
rs3100127 		1 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.010 1.000 1 2016 2016
dbSNP: rs386231
rs386231
NOS1AP
4 0.882 0.080 1 162356033 intron variant C/T snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs4511180
rs4511180
PTPRVP
1 1.000 0.040 1 202180311 non coding transcript exon variant A/G snv 0.65 0.700 1.000 1 2015 2015
dbSNP: rs4606
rs4606
RGS2
16 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs562010289
rs562010289
LAMC2
2 0.925 0.120 1 183227583 missense variant G/A;C snv 1.7E-04 0.010 1.000 1 2010 2010
dbSNP: rs7552841
rs7552841
PCSK9
3 0.925 0.160 1 55053079 intron variant C/T snv 0.32 0.010 1.000 1 2017 2017
dbSNP: rs10170218
rs10170218 		1 1.000 0.040 2 187949717 intron variant A/C snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs1143633
rs1143633
IL1B
11 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs16944
rs16944
IL1B
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
dbSNP: rs3749034
rs3749034
GAD1
6 0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs523349
rs523349
SRD5A2
21 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 0.010 1.000 1 2013 2013
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.030 1.000 3 2017 2020
dbSNP: rs1799923
rs1799923
CCK
2 0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 0.010 1.000 1 2015 2015
dbSNP: rs2251177
rs2251177
DRD3
1 1.000 0.040 3 114139503 missense variant C/A;T snv 8.0E-06; 0.99 0.010 1.000 1 2014 2014
dbSNP: rs2254298
rs2254298
CAV3 ; OXTR
23 0.701 0.200 3 8760542 intron variant G/A snv 0.16 0.010 1.000 1 2019 2019
dbSNP: rs2268498
rs2268498
CAV3 ; OXTR
7 0.827 0.080 3 8770725 intron variant T/C snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs495225
rs495225
GHSR
4 0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 0.010 1.000 1 2019 2019