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: rs10038095
rs10038095
HMGCR
3 5 75341886 intron variant A/T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs1006725
rs1006725
TCF7L2
2 10 112970444 intron variant A/G snv 4.2E-03 0.700 1.000 1 2012 2012
dbSNP: rs10087178
rs10087178
MSRA
2 8 10111284 intron variant T/C snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10102164
rs10102164
RP1
4 8 54509054 upstream gene variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs10107815
rs10107815
MSRA
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10156121
rs10156121 		4 7 142672656 downstream gene variant T/C snv 3.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs10199768
rs10199768
APOB
5 2 21021128 intron variant G/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs10212320
rs10212320
TGFBR2
2 3 30632373 non coding transcript exon variant C/T snv 7.2E-03 0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10260606
rs10260606 		3 7 44544952 upstream gene variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
NAMPT
4 7 106258428 intron variant C/T snv 5.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10306121
rs10306121
PTGS1
2 9 122372369 intron variant A/T snv 6.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs10306137
rs10306137
PTGS1
3 9 122376185 intron variant C/T snv 1.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 5 2009 2013
dbSNP: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.700 1.000 2 2008 2012
dbSNP: rs10402729
rs10402729
NCAN
4 19 19244291 intron variant T/C snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs10415849
rs10415849
GATAD2A
4 19 19394278 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1041968
rs1041968
APOB
6 2 21009932 synonymous variant G/A snv 0.39 0.38 0.700 1.000 1 2012 2012
dbSNP: rs1042031
rs1042031
APOB
11 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 0.700 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 0.700 1.000 1 2012 2012
dbSNP: rs10433493
rs10433493
IL1RAP
2 3 190647811 intron variant G/C snv 1.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 2 2012 2012
dbSNP: rs10474434
rs10474434
HMGCR
3 5 75348856 intron variant G/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs10478730
rs10478730
EDN1
5 6 12297276 downstream gene variant C/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
4 6 131578846 intron variant C/T snv 3.3E-02 0.700 1.000 1 2012 2012