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: rs9979383
rs9979383
RUNX1
5 0.925 0.200 21 35343463 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs990171
rs990171 		2 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 0.800 1.000 1 2011 2011
dbSNP: rs9873580
rs9873580
IL12A-AS1
1 1.000 0.080 3 159911578 non coding transcript exon variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs9792269
rs9792269 		5 0.882 0.200 8 128252343 intergenic variant A/C;G snv 0.800 1.000 1 2010 2010
dbSNP: rs971290
rs971290 		1 1.000 0.080 14 68805252 intergenic variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9491896
rs9491896
PTPRK
1 1.000 0.080 6 127979804 intron variant G/A snv 8.5E-02 0.010 1.000 1 2014 2014
dbSNP: rs947474
rs947474
LINC02649 ; LINC02656
5 0.827 0.440 10 6348488 intron variant G/A snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs9457515
rs9457515
C6orf99
1 1.000 0.080 6 158913093 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs9391227
rs9391227 		1 1.000 0.080 6 104710759 regulatory region variant T/A snv 0.56 0.010 1.000 1 2011 2011
dbSNP: rs936229
rs936229
ULK3
2 1.000 0.080 15 74839978 intron variant A/G snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs9357152
rs9357152 		5 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 0.700 1.000 1 2007 2007
dbSNP: rs9286879
rs9286879 		4 0.851 0.200 1 172893094 intron variant A/G snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs9275141
rs9275141 		6 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs917997
rs917997 		20 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 0.830 1.000 4 2009 2015
dbSNP: rs888208
rs888208
NKX2-3
3 0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25 0.010 1.000 1 2009 2009
dbSNP: rs879761216
rs879761216
CNR2
14 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 0.020 1.000 2 2012 2018
dbSNP: rs864537
rs864537
CD247
4 0.925 0.200 1 167442147 intron variant A/G snv 0.29 0.800 1.000 1 2010 2010
dbSNP: rs859715
rs859715 		1 1.000 0.080 1 172790982 intron variant A/T snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs855791
rs855791
TMPRSS6
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs842647
rs842647
REL
6 0.827 0.400 2 60892336 intron variant G/A snv 0.62 0.010 1.000 1 2009 2009
dbSNP: rs8081319
rs8081319
ACACA ; C17orf78
1 1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 0.800 1.000 1 2014 2014
dbSNP: rs80356624
rs80356624
KCNJ11
16 0.752 0.240 11 17387490 missense variant C/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs802734
rs802734 		7 0.827 0.280 6 127957653 intergenic variant A/G;T snv 0.810 1.000 2 2010 2014
dbSNP: rs80209296
rs80209296
PTPN2
2 0.925 0.200 18 12860802 intron variant G/A snv 0.700 1.000 1 2016 2016