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: rs3184504
rs3184504
ATXN2 ; SH2B3
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.800 1.000 2 2011 2018
dbSNP: rs12518099
rs12518099
LINC01339
3 0.925 0.120 5 90250292 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
23 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs5167
rs5167
APOC2 ; APOC4 ; APOC4-APOC2
7 1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 0.700 1.000 1 2009 2009
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs763361
rs763361
CD226
21 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 0.700 1.000 1 2011 2011
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12722495
rs12722495
IL2RA
5 0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs1048699
rs1048699
MARK4 ; PPP1R37
2 1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs8103315
rs8103315
BCL3
2 1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs1114832
rs1114832
MARK4 ; PPP1R37
2 1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs3024505
rs3024505 		10 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2009 2009
dbSNP: rs12610605
rs12610605
NECTIN2
2 1.000 0.080 19 44867581 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs2927438
rs2927438 		6 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs2304256
rs2304256
TYK2
13 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 0.700 1.000 1 2011 2011
dbSNP: rs7171171
rs7171171
LOC107984725
3 0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs2069762
rs2069762
IL2
23 0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1701704
rs1701704
IKZF4 ; LOC105369781
5 0.851 0.200 12 56018703 intron variant T/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs1871047
rs1871047
NECTIN2
2 1.000 0.080 19 44848489 intron variant A/G snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs377702
rs377702
NECTIN2
2 1.000 0.080 19 44859410 intron variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2965101
rs2965101 		6 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs8106922
rs8106922
TOMM40
5 1.000 0.080 19 44898409 intron variant A/G snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs4788084
rs4788084
IL27
6 0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 0.700 1.000 1 2011 2011