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: rs10175338
rs10175338
CYP1B1 ; CYP1B1-AS1
2 0.925 0.080 2 38080501 intron variant G/T snv 0.25 0.010 1.000 1 2017 2017
dbSNP: rs10204525
rs10204525
PDCD1
20 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2016 2016
dbSNP: rs1020475809
rs1020475809
NQO1
2 0.925 0.080 16 69711027 synonymous variant A/G snv 2.0E-05 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs10216653
rs10216653
CHRAC1
3 0.882 0.080 8 140516886 3 prime UTR variant G/C snv 0.80 0.010 1.000 1 2017 2017
dbSNP: rs10235235
rs10235235
ZNF394 ; ZNF789
4 0.925 0.080 7 99478208 intron variant T/C snv 0.13 0.010 1.000 1 2014 2014
dbSNP: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs10269006
rs10269006 		1 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs10273424
rs10273424
TMEM225B
3 0.925 0.080 7 99598450 intron variant T/A snv 0.13 0.010 1.000 1 2012 2012
dbSNP: rs1028842
rs1028842
RAD51B
1 1.000 0.080 14 68205006 intron variant C/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs1029342144
rs1029342144
PTEN ; KLLN
6 0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs1029946
rs1029946
PRKAG2
2 0.925 0.080 7 151578720 intron variant A/G snv 0.21 0.010 1.000 1 2013 2013
dbSNP: rs1033662
rs1033662
LINC01524 ; LOC105372666
2 0.925 0.080 20 52408842 intron variant A/G snv 0.46 0.010 1.000 1 2018 2018
dbSNP: rs1034794
rs1034794 		2 0.925 0.080 7 124801348 intergenic variant A/T snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs1036980234
rs1036980234
PTCH1
6 0.827 0.160 9 95447156 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs10380
rs10380
MTRR
6 0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 0.010 1.000 1 2014 2014
dbSNP: rs1038304
rs1038304
CCDC170 ; LOC107986528
4 0.882 0.160 6 151612040 intron variant A/G snv 0.58 0.010 1.000 1 2011 2011
dbSNP: rs1039659576
rs1039659576
MTR
21 0.689 0.520 1 236803473 missense variant A/G snv 0.010 1.000 1 2012 2012
dbSNP: rs1041981
rs1041981
LTA ; LOC100287329
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.010 1.000 1 2014 2014
dbSNP: rs1041983
rs1041983
NAT2
15 0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 0.010 1.000 1 2016 2016
dbSNP: rs1042028
rs1042028
SULT1A1
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.100 0.800 10 2004 2015
dbSNP: rs1042031
rs1042031
APOB
11 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 0.010 1.000 1 2013 2013
dbSNP: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.833 48 2003 2020
dbSNP: rs1042638
rs1042638
TPD52
2 0.925 0.080 8 80037711 3 prime UTR variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2012 2019
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.010 1.000 1 2012 2012