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: rs11813268
rs11813268 		2 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs132793
rs132793 		7 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1417080
rs1417080 		2 0.925 0.120 9 79515946 non coding transcript exon variant T/C snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs3118523
rs3118523 		2 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 0.010 1.000 1 2009 2009
dbSNP: rs6466135
rs6466135 		2 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 0.010 1.000 1 2018 2018
dbSNP: rs7132434
rs7132434 		2 0.925 0.120 12 26319629 non coding transcript exon variant A/G snv 0.62 0.010 1.000 1 2016 2016
dbSNP: rs748964
rs748964 		2 0.925 0.120 9 134442243 downstream gene variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs7859384
rs7859384 		6 0.882 0.120 9 79507370 intron variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2231142
rs2231142
ABCG2
56 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2005 2005
dbSNP: rs1154454
rs1154454
ADH7
2 0.925 0.120 4 99417185 intron variant A/G snv 0.22 0.010 < 0.001 1 2018 2018
dbSNP: rs182052
rs182052
ADIPOQ
19 0.701 0.440 3 186842993 intron variant G/A snv 0.38 0.020 1.000 2 2015 2018
dbSNP: rs266729
rs266729
ADIPOQ
37 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3774262
rs3774262
ADIPOQ ; ADIPOQ-AS1
5 0.851 0.200 3 186854025 intron variant G/A snv 0.10 0.010 1.000 1 2015 2015
dbSNP: rs1800435
rs1800435
ALAD
7 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs2761016
rs2761016
ALAD
2 0.925 0.120 9 113391072 intron variant T/C snv 0.59 0.010 1.000 1 2011 2011
dbSNP: rs1048798213
rs1048798213
APC
1 1.000 0.120 5 112837872 missense variant C/G snv 0.010 1.000 1 2019 2019
dbSNP: rs1442780982
rs1442780982
APC
1 1.000 0.120 5 112837977 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1130409
rs1130409
APEX1
72 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 0.010 1.000 1 2011 2011
dbSNP: rs1760944
rs1760944
APEX1 ; OSGEP
26 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.010 1.000 1 2015 2015
dbSNP: rs2606736
rs2606736
ATG7
4 1.000 0.120 3 11358775 intron variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs6442260
rs6442260
ATG7
2 0.925 0.160 3 11549277 intron variant G/A snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs611646
rs611646
ATM
3 0.882 0.120 11 108306370 intron variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs750597831
rs750597831
ATM
2 1.000 0.120 11 108229230 missense variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs587782274
rs587782274
ATM ; C11orf65
1 1.000 0.120 11 108312465 missense variant A/C snv 0.700 0