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: rs999556
rs999556 		2 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs9988642
rs9988642
IL23R
3 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 0.800 1.000 1 2012 2012
dbSNP: rs9987128
rs9987128
CSMD1
1 1.000 0.040 8 3122601 intron variant A/G snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs9977672
rs9977672 		10 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs9952991
rs9952991 		2 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs9889296
rs9889296 		6 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs984473166
rs984473166
SSTR4
1 1.000 0.040 20 23035661 missense variant G/T snv 0.010 1.000 1 2007 2007
dbSNP: rs982610810
rs982610810
TNF
1 1.000 0.040 6 31575766 missense variant G/A snv 4.2E-06 0.010 1.000 1 2013 2013
dbSNP: rs9808753
rs9808753
IFNGR2
17 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 0.700 1.000 1 2015 2015
dbSNP: rs9807841
rs9807841
QTRT1
1 1.000 0.040 19 10706980 intron variant T/C snv 0.73 0.700 1.000 1 2015 2015
dbSNP: rs9797244
rs9797244
NOS2
5 0.827 0.120 17 27770105 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs9687958
rs9687958 		6 0.827 0.120 5 40496321 intron variant G/T snv 0.60 0.700 1.000 1 2016 2016
dbSNP: rs963986
rs963986
CAVIN1
1 1.000 0.040 17 42409561 intron variant G/C snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs9554587
rs9554587 		5 0.827 0.120 13 99388400 downstream gene variant A/G snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs955155
rs955155 		1 1.000 0.040 19 39238839 upstream gene variant G/A snv 0.20 0.010 1.000 1 2012 2012
dbSNP: rs953861
rs953861
LOC285626
1 1.000 0.040 5 159345574 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs9533962
rs9533962 		1 1.000 0.040 13 44760058 regulatory region variant C/T snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs953038635
rs953038635
SOD2
51 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 0.010 < 0.001 1 2014 2014
dbSNP: rs9513593
rs9513593
GPR183 ; UBAC2
1 1.000 0.040 13 99298006 intron variant G/A snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs9504361
rs9504361
EXOC2
3 1.000 0.040 6 577820 intron variant A/G snv 0.40 0.800 1.000 2 2012 2015
dbSNP: rs9494840
rs9494840 		5 0.827 0.120 6 137641937 regulatory region variant T/A snv 4.3E-05 0.700 1.000 1 2016 2016
dbSNP: rs9491891
rs9491891 		5 0.827 0.120 6 127956006 intergenic variant A/G snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs9487605
rs9487605
MFSD4B
1 1.000 0.040 6 111261682 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs9481169
rs9481169 		1 1.000 0.040 6 111608659 upstream gene variant G/T snv 0.17 0.700 1.000 1 2015 2015