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: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2012 2012
dbSNP: rs2239612
rs2239612
ST6GAL1
2 1.000 0.040 3 187075454 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs2239815
rs2239815
XBP1
3 0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs2847281
rs2847281
PTPN2
3 1.000 0.040 18 12821594 intron variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs35063026
rs35063026
SPATA33
3 0.925 0.080 16 89669749 3 prime UTR variant C/T snv 4.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs35324266
rs35324266 		1 1.000 0.040 6 32625467 upstream gene variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs35407
rs35407
SLC45A2
6 0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3846662
rs3846662
HMGCR
12 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.700 1.000 1 2012 2012
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs4149056
rs4149056
SLCO1B1
45 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 0.700 1.000 1 2012 2012
dbSNP: rs4268748
rs4268748
DEF8
3 0.925 0.080 16 89960104 intron variant T/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs4299376
rs4299376
ABCG8 ; LOC102725159
11 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4455710
rs4455710
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
1 1.000 0.040 6 32641081 intron variant C/T snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs4761496
rs4761496 		4 0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs4785204
rs4785204
HEATR3
2 1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs4803750
rs4803750
BCL3
22 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs4822983
rs4822983
CHEK2
3 0.925 0.080 22 28719078 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs6059655
rs6059655
RALY
10 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2016 2016
dbSNP: rs62209647
rs62209647 		1 1.000 0.040 20 33917852 upstream gene variant G/C snv 4.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs62246017
rs62246017
FOXP1
1 1.000 0.040 3 71433933 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs646776
rs646776
CELSR2
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012
dbSNP: rs6503659
rs6503659 		2 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6511720
rs6511720
LDLR
15 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs6743068
rs6743068
FLACC1
1 1.000 0.040 2 201289197 intron variant A/G snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs6791479
rs6791479 		1 1.000 0.040 3 189487243 intergenic variant T/A snv 0.48 0.700 1.000 1 2016 2016