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: rs2267735
rs2267735
ADCYAP1R1
2 0.925 0.120 7 31095890 intron variant C/G snv 0.47 0.050 0.800 5 2013 2017
dbSNP: rs2400707
rs2400707
ADRB2
3 1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 0.020 1.000 2 2014 2017
dbSNP: rs10744891
rs10744891
NOS1
1 1.000 0.040 12 117284536 intron variant G/T snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs110402
rs110402
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.010 1.000 1 2017 2017
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: rs1187327
rs1187327
NTRK2
1 1.000 0.040 9 84673625 intron variant T/C snv 0.50 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: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2017 2017
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: rs7208505
rs7208505
SKA2
2 1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 0.020 0.500 2 2016 2016
dbSNP: rs1374141592
rs1374141592
FLT4
1 1.000 0.040 5 180630561 missense variant C/T snv 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs159572
rs159572
ANKRD55
1 1.000 0.040 5 56211219 intron variant A/C snv 0.37 0.700 1.000 1 2016 2016
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: rs10144436
rs10144436
DICER1
1 1.000 0.040 14 95090065 3 prime UTR variant C/A snv 2.9E-02 0.010 1.000 1 2015 2015
dbSNP: rs1033962
rs1033962
PRTFDC1
1 1.000 0.040 10 24927877 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs1042357
rs1042357
ALOX12 ; ALOX12-AS1
2 0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs10852889
rs10852889
ALOX12 ; ALOX12-AS1
1 1.000 0.040 17 6997526 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
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: rs12898919
rs12898919
CHRNA5
1 1.000 0.040 15 78588235 intron variant G/C snv 3.1E-02 0.010 1.000 1 2015 2015
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: rs2075652
rs2075652
DRD2
1 1.000 0.040 11 113424176 intron variant G/A snv 4.2E-02 0.010 1.000 1 2015 2015
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: rs356195
rs356195
SNCA
1 1.000 0.040 4 89762017 intron variant T/C snv 0.81 0.010 1.000 1 2015 2015
dbSNP: rs4311
rs4311
ACE
3 0.882 0.200 17 63483402 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
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