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 0.800 1.000 3 2012 2019
dbSNP: rs10045497
rs10045497
HMGCR
2 5 75340659 intron variant C/A snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs10054063
rs10054063 		4 5 173965395 downstream gene variant A/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10066168
rs10066168
HAVCR1
2 5 157057207 intron variant C/G;T snv 0.700 1.000 1 2019 2019
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 0.800 1.000 4 2013 2019
dbSNP: rs10104003
rs10104003
RP1
1 8 54509880 intron variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs10107815
rs10107815
MSRA
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10128711
rs10128711
SPTY2D1
2 11 18611437 intron variant T/C snv 0.64 0.55 0.700 1.000 1 2018 2018
dbSNP: rs1014283
rs1014283
ABCB4
2 7 87447271 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10156121
rs10156121 		4 7 142672656 downstream gene variant T/C snv 3.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs1016988
rs1016988 		4 5 132408882 upstream gene variant T/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10172650
rs10172650 		2 2 20982585 intergenic variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs10176901
rs10176901
ABCB11
2 2 168974151 intron variant G/A snv 0.57 0.700 1.000 2 2019 2019
dbSNP: rs10185855
rs10185855
TBC1D8
4 2 101025798 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs10199768
rs10199768
APOB
5 2 21021128 intron variant G/T snv 0.35 0.800 1.000 2 2011 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 0.800 1.000 2 2012 2018
dbSNP: rs10271556
rs10271556
NAMPT
4 7 106258428 intron variant C/T snv 5.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10275712
rs10275712
C7orf50 ; GPR146
1 7 1043282 intron variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs1030431
rs1030431 		3 8 58399138 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
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