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: rs10044254
rs10044254
FBXL7
2 0.925 0.080 5 15783487 intron variant A/G snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs10494132
rs10494132
CHIA
4 0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs10519031
rs10519031 		1 1.000 0.080 15 59890806 regulatory region variant T/C snv 2.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.010 1.000 1 2013 2013
dbSNP: rs10830123
rs10830123
NPS
1 1.000 0.080 10 127551386 intron variant G/C snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs121912633
rs121912633
TRPV4
10 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1220579705
rs1220579705
IL4
1 1.000 0.080 5 132674079 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs12603332
rs12603332
ORMDL3 ; LRRC3C ; LOC112268187
7 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 0.010 1.000 1 2019 2019
dbSNP: rs1342326
rs1342326 		9 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.010 1.000 1 2018 2018
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs16917204
rs16917204
BDNF-AS
5 0.827 0.160 11 27646808 intron variant G/C snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs1800470
rs1800470
TGFB1
107 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2009 2009
dbSNP: rs1800471
rs1800471
TGFB1
48 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2017 2017
dbSNP: rs1800888
rs1800888
ADRB2
23 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2013 2013
dbSNP: rs1801275
rs1801275
IL4R
58 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 0.010 1.000 1 2016 2016
dbSNP: rs1805011
rs1805011
IL4R
8 0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 0.010 1.000 1 2009 2009
dbSNP: rs1859430
rs1859430
IL9
2 0.925 0.080 5 135894824 intron variant G/A snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs1931704
rs1931704 		1 1.000 0.080 10 127541545 intergenic variant G/A snv 0.28 0.010 1.000 1 2017 2017
dbSNP: rs1999071
rs1999071 		4 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs20541
rs20541
IL13 ; TH2LCRR
52 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 0.010 1.000 1 2016 2016
dbSNP: rs2069885
rs2069885
IL9
5 0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 0.010 1.000 1 2015 2015
dbSNP: rs2070874
rs2070874
IL4
27 0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 0.010 1.000 1 2015 2015