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: rs10065633
rs10065633
IRF1-AS1
1 1.000 0.040 5 132481024 intron variant T/C snv 0.38 0.010 1.000 1 2008 2008
dbSNP: rs10251201
rs10251201
UMAD1
4 0.851 0.160 7 7932654 intron variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs10405859
rs10405859
MARK4 ; PPP1R37
3 0.882 0.080 19 45099523 intron variant T/C snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs10740055
rs10740055
ARID5B
7 0.790 0.240 10 61958720 intron variant C/A snv 0.49 0.010 1.000 1 2019 2019
dbSNP: rs10821936
rs10821936
ARID5B
11 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2017 2017
dbSNP: rs10931910
rs10931910
AOX1
2 0.925 0.040 2 200659013 intron variant A/G;T snv 0.010 < 0.001 1 2014 2014
dbSNP: rs11079041
rs11079041
STAT5B
4 0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs113017087
rs113017087
APC
1 1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 0.010 1.000 1 2016 2016
dbSNP: rs17886724
rs17886724
STAT3
2 0.925 0.040 17 42344145 intron variant A/G snv 0.35 0.010 1.000 1 2012 2012
dbSNP: rs2234693
rs2234693
ESR1
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
dbSNP: rs2293157
rs2293157
STAT5A
9 0.763 0.120 17 42300657 intron variant C/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs2413739
rs2413739
PACSIN2
6 0.827 0.120 22 43001030 intron variant C/T snv 0.43 0.010 1.000 1 2012 2012
dbSNP: rs3116496
rs3116496
CD28
11 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2019 2019
dbSNP: rs4938723
rs4938723
BTG4 ; MIR34B ; MIR34C ; LOC728196
60 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2018 2018
dbSNP: rs6964823
rs6964823
IKZF1
3 0.925 0.040 7 50392398 intron variant G/A snv 0.45 0.010 1.000 1 2019 2019
dbSNP: rs7090445
rs7090445
ARID5B
2 0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 0.010 1.000 1 2019 2019
dbSNP: rs75612255
rs75612255
APC
1 1.000 0.040 5 112737543 intron variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs9318227
rs9318227
KLF12
3 0.882 0.080 13 73926833 intron variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs974120
rs974120 		4 0.851 0.200 8 2789080 intron variant T/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs387906659
rs387906659
AKT2
14 0.742 0.280 19 40257052 stop gained C/A;T snv 0.020 1.000 2 2007 2008
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 1.000 1 2015 2015
dbSNP: rs562015640
rs562015640
PTEN
16 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs121913459
rs121913459
ABL1
25 0.672 0.160 9 130872896 missense variant C/T snv 0.100 1.000 18 2004 2018
dbSNP: rs77375493
rs77375493
JAK2 ; INSL6
187 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 1.000 10 2006 2017
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.070 1.000 7 2001 2016