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: rs10013040
rs10013040
NEIL3
1 1.000 0.080 4 177309998 synonymous variant C/A snv 0.20 0.20 0.010 < 0.001 1 2015 2015
dbSNP: rs1007888
rs1007888
MIF-AS1
4 0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 0.010 1.000 1 2009 2009
dbSNP: rs1008563
rs1008563 		1 1.000 0.080 2 218162165 downstream gene variant G/A snv 0.43 0.010 1.000 1 2014 2014
dbSNP: rs10118757
rs10118757
MTAP
7 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 < 0.001 1 2013 2013
dbSNP: rs1012841819
rs1012841819
ADRA2B
4 0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1024323
rs1024323
GRK4
4 0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs10304
rs10304
SMTN ; SELENOM
2 0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 0.010 1.000 1 2012 2012
dbSNP: rs1041740
rs1041740
SOD1
8 0.807 0.320 21 31667849 intron variant C/T snv 0.24 0.010 1.000 1 2012 2012
dbSNP: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.010 1.000 1 2004 2004
dbSNP: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2012 2012
dbSNP: rs10432782
rs10432782
SOD1
7 0.807 0.160 21 31664078 intron variant T/G snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs104895285
rs104895285
TNFRSF1A
1 1.000 0.080 12 6330873 missense variant A/T snv 0.010 1.000 1 2008 2008
dbSNP: rs1049636
rs1049636
FGG
1 1.000 0.080 4 154604818 3 prime UTR variant G/A snv 0.67 0.70 0.010 1.000 1 2007 2007
dbSNP: rs10507391
rs10507391
ALOX5AP
10 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 1.000 1 2019 2019
dbSNP: rs1050998
rs1050998
CXCL16
1 1.000 0.080 17 4735442 missense variant A/G snv 0.46 0.41 0.010 1.000 1 2017 2017
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 < 0.001 1 2015 2015
dbSNP: rs1053874
rs1053874
DNASE1 ; TRAP1
7 0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs1057335
rs1057335
SERPINF2
5 0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 0.010 < 0.001 1 2011 2011
dbSNP: rs1058932
rs1058932
CYP2C8
1 1.000 0.080 10 95037104 3 prime UTR variant G/A snv 0.22 0.24 0.010 1.000 1 2010 2010
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1063537
rs1063537
ADIPOQ ; ADIPOQ-AS1
6 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 0.010 1.000 1 2013 2013
dbSNP: rs1063539
rs1063539
ADIPOQ ; ADIPOQ-AS1
5 0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10 0.010 1.000 1 2013 2013
dbSNP: rs10733113
rs10733113 		3 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 0.010 1.000 1 2016 2016
dbSNP: rs10738605
rs10738605
CDKN2B-AS1
3 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs10741657
rs10741657
CYP2R1
34 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2015 2015