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: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2011 2012
dbSNP: rs939481814
rs939481814
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A1 ; UGT1A3
1 2 233767063 synonymous variant A/T snv 0.010 1.000 1 2009 2009
dbSNP: rs878854066
rs878854066
TP53
213 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2006 2006
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs7968585
rs7968585
LINC02354
7 0.851 0.160 12 47838310 downstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs7873784
rs7873784
TLR4
11 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs7837328
rs7837328
POU5F1B ; CASC8 ; PCAT1
8 0.882 0.120 8 127410882 intron variant A/G snv 0.52 0.010 1.000 1 2008 2008
dbSNP: rs778826879
rs778826879
MAPK3
3 16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs775144154
rs775144154
SLC19A1
38 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 0.010 1.000 1 2011 2011
dbSNP: rs774679649
rs774679649
CRP
1 1 159713878 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs770460061
rs770460061
GSTP1
14 0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs763539313
rs763539313
GAPDH
1 12 6537702 missense variant A/G snv 2.0E-05 4.9E-05 0.010 1.000 1 2005 2005
dbSNP: rs756363791
rs756363791
OGG1
4 0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 0.010 1.000 1 2011 2011
dbSNP: rs746497256
rs746497256
NFE2L2
3 0.925 0.080 2 177231925 synonymous variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2017 2017
dbSNP: rs719725
rs719725 		7 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 0.010 < 0.001 1 2010 2010
dbSNP: rs7131056
rs7131056
DRD2
6 0.827 0.200 11 113459052 intron variant A/C snv 0.51 0.010 1.000 1 2016 2016
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.030 1.000 3 2008 2019
dbSNP: rs6586714
rs6586714
NAT1
2 1.000 8 18216433 intron variant A/G snv 0.84 0.010 1.000 1 2012 2012
dbSNP: rs6471
rs6471
CYP21A2
24 0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 0.010 1.000 1 1998 1998
dbSNP: rs61734277
rs61734277
GCM2
5 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 0.010 1.000 1 2019 2019
dbSNP: rs5789
rs5789
PTGS1
2 1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 0.010 < 0.001 1 2004 2004
dbSNP: rs55819519
rs55819519
TP53
40 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 0.010 1.000 1 1999 1999
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2005 2005
dbSNP: rs536562413
rs536562413
MSH6 ; FBXO11
15 0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 0.010 1.000 1 2006 2006