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: rs2981579
rs2981579
FGFR2
8 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.740 1.000 9 2009 2017
dbSNP: rs1011970
rs1011970
CDKN2B-AS1
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.730 1.000 8 2010 2017
dbSNP: rs2420946
rs2420946
FGFR2
4 0.851 0.160 10 121591810 intron variant T/C snv 0.56 0.770 1.000 8 2009 2017
dbSNP: rs796065354
rs796065354
ESR1
9 0.882 0.080 6 151944320 missense variant A/G snv 0.080 1.000 8 2004 2010
dbSNP: rs12443621
rs12443621
TOX3
6 0.807 0.120 16 52514125 intron variant A/G snv 0.48 0.070 0.857 7 2009 2016
dbSNP: rs1292011
rs1292011
LOC105370003
4 0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 0.740 1.000 7 2012 2017
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.070 0.714 7 2009 2019
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.720 1.000 7 2013 2017
dbSNP: rs8051542
rs8051542
TOX3
2 0.925 0.080 16 52500255 intron variant T/C snv 0.61 0.070 0.857 7 2010 2019
dbSNP: rs9340799
rs9340799
ESR1
62 0.583 0.680 6 151842246 intron variant A/G snv 0.32 0.070 0.857 7 2007 2020
dbSNP: rs1258159645
rs1258159645
NQO1
37 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.060 0.833 6 2004 2016
dbSNP: rs1799794
rs1799794
KLC1 ; XRCC3
12 0.763 0.320 14 103712930 splice region variant T/C snv 0.22 0.060 0.667 6 2011 2017
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
dbSNP: rs1801157
rs1801157
CXCL12
46 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 0.060 1.000 6 2009 2017
dbSNP: rs2588809
rs2588809
RAD51B
6 0.807 0.160 14 68193711 intron variant T/C snv 0.80 0.820 1.000 6 2012 2017
dbSNP: rs2823093
rs2823093 		3 0.882 0.080 21 15148511 intergenic variant G/A snv 0.32 0.730 0.833 6 2012 2017
dbSNP: rs3757318
rs3757318
CCDC170
3 0.882 0.160 6 151592978 intron variant G/A snv 6.1E-02 0.740 1.000 6 2013 2016
dbSNP: rs3798577
rs3798577
ESR1
16 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 0.060 1.000 6 2009 2018
dbSNP: rs704010
rs704010
ZMIZ1
4 0.851 0.080 10 79081391 intron variant T/C snv 0.71 0.720 1.000 6 2010 2017
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.060 1.000 6 2012 2018
dbSNP: rs865686
rs865686
LOC105376214
4 0.851 0.080 9 108126198 regulatory region variant G/A;T snv 0.740 1.000 6 2011 2016
dbSNP: rs11075995
rs11075995
FTO
5 0.882 0.080 16 53821379 intron variant A/T snv 0.77 0.720 1.000 5 2013 2017
dbSNP: rs12255372
rs12255372
TCF7L2
28 0.667 0.480 10 113049143 intron variant G/A;T snv 0.050 1.000 5 2008 2018
dbSNP: rs1432679
rs1432679
EBF1
4 0.851 0.080 5 158817075 intron variant C/T snv 0.44 0.720 1.000 5 2013 2017
dbSNP: rs1562430
rs1562430
POU5F1B ; CASC8 ; PCAT1 ; CASC21
6 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.730 1.000 5 2010 2015