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: rs1329149
rs1329149
CYP2E1
2 0.925 0.080 10 133536297 intron variant T/C snv 0.73 0.020 1.000 2 2009 2012
dbSNP: rs1052748
rs1052748
PLD2
2 0.925 0.080 17 4817174 missense variant C/T snv 0.39 0.36 0.010 1.000 1 2003 2003
dbSNP: rs1063169
rs1063169
FOS
2 0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1065411
rs1065411
GSTM1 ; GSTM2
2 0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 0.010 1.000 1 2010 2010
dbSNP: rs10845671
rs10845671
GPRC5D-AS1
2 0.925 0.080 12 12926708 upstream gene variant C/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs10883782
rs10883782
WBP1L
2 0.925 0.080 10 102824175 intron variant A/G snv 0.14 0.010 1.000 1 2011 2011
dbSNP: rs11568591
rs11568591
ABCC3
2 0.925 0.080 17 50683692 missense variant G/A snv 3.7E-02 3.9E-02 0.010 1.000 1 2008 2008
dbSNP: rs116896264
rs116896264
LGALS4
2 0.925 0.080 19 38813176 upstream gene variant G/T snv 9.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs11704
rs11704
CINP ; ZNF839
2 0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs1176119168
rs1176119168
HSPA1B
2 0.925 0.080 6 31828202 missense variant G/A;T snv 1.9E-05 0.010 1.000 1 2007 2007
dbSNP: rs118049207
rs118049207
SND1
2 0.925 0.080 7 127890817 intron variant A/G snv 1.7E-03 0.010 1.000 1 2020 2020
dbSNP: rs1215486792
rs1215486792
MOK
2 0.925 0.080 14 102229572 missense variant C/G snv 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs12373
rs12373
ZG16B
2 0.925 0.080 16 2832196 3 prime UTR variant G/T snv 0.66 0.63 0.010 1.000 1 2015 2015
dbSNP: rs12477554
rs12477554
TACR1 ; LOC105374811 ; LOC105374812
2 0.925 0.080 2 75174939 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1282801317
rs1282801317
EGFR
2 0.925 0.080 7 55143316 missense variant G/C snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs13072632
rs13072632
CTNNB1
2 0.925 0.080 3 41220953 5 prime UTR variant T/C snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs1330586270
rs1330586270
EPHB2
2 0.925 0.080 1 22882367 missense variant G/A snv 0.010 1.000 1 2008 2008
dbSNP: rs1367801477
rs1367801477
ACD ; CARMIL2
2 0.925 0.080 16 67657673 missense variant T/C snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs1376199019
rs1376199019
CYP1A1
2 0.925 0.080 15 74720557 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs141178472
rs141178472
PIK3CA
2 0.925 0.080 3 179234393 3 prime UTR variant T/C snv 3.0E-03 3.3E-03 0.010 1.000 1 2015 2015
dbSNP: rs1419316960
rs1419316960
DNMT1
2 0.925 0.080 19 10166651 missense variant T/C snv 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1466012753
rs1466012753
MLH1
2 0.925 0.080 3 37014525 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs147079820
rs147079820
KIF2C
2 0.925 0.080 1 44758123 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs149418249
rs149418249
ACD ; CARMIL2
2 0.925 0.080 16 67657798 missense variant G/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1725459
rs1725459
SIPA1L3
2 0.925 0.080 19 38049092 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019