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: rs6733839
rs6733839
LOC105373605
2 1.000 0.080 2 127135234 regulatory region variant C/T snv 0.39 0.820 1.000 8 2013 2019
dbSNP: rs9331896
rs9331896
CLU ; MIR6843
4 0.851 0.080 8 27610169 intron variant C/G;T snv 0.820 1.000 6 2013 2019
dbSNP: rs7561528
rs7561528
LOC105373605
3 0.882 0.080 2 127132061 intergenic variant G/A snv 0.28 0.820 1.000 5 2011 2017
dbSNP: rs2718058
rs2718058
EPDR1 ; GPR141
2 0.925 0.080 7 37801932 intron variant A/G;T snv 0.820 1.000 4 2013 2019
dbSNP: rs10838725
rs10838725
CELF1
2 0.925 0.160 11 47536319 intron variant T/C snv 0.22 0.820 1.000 3 2013 2018
dbSNP: rs11754661
rs11754661
MTHFD1L
6 0.851 0.120 6 150885942 intron variant G/A;T snv 0.820 0.667 3 2010 2011
dbSNP: rs157580
rs157580
TOMM40
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.810 1.000 14 2009 2019
dbSNP: rs439401
rs439401 		8 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 0.810 1.000 12 2009 2019
dbSNP: rs6857
rs6857
NECTIN2
16 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 0.810 1.000 9 2009 2017
dbSNP: rs157582
rs157582
TOMM40
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.810 1.000 7 2010 2019
dbSNP: rs11771145
rs11771145
EPHA1-AS1
2 0.925 0.080 7 143413669 intron variant G/A snv 0.42 0.810 1.000 6 2011 2019
dbSNP: rs9271192
rs9271192 		1 1.000 0.080 6 32610753 intergenic variant C/A snv 0.74 0.810 1.000 5 2013 2019
dbSNP: rs7920721
rs7920721
LOC105376412 ; LOC105376413
1 1.000 0.080 10 11678309 upstream gene variant A/G snv 0.31 0.810 1.000 4 2013 2019
dbSNP: rs6701713
rs6701713
CR1
1 1.000 0.080 1 207612944 intron variant A/G;T snv 0.810 1.000 3 2011 2018
dbSNP: rs11767557
rs11767557
EPHA1-AS1
4 0.882 0.080 7 143412046 intron variant T/C snv 0.18 0.810 1.000 2 2011 2018
dbSNP: rs12989701
rs12989701
LOC105373605
1 1.000 0.080 2 127130409 regulatory region variant C/A snv 0.13 0.810 1.000 2 2011 2017
dbSNP: rs1466662
rs1466662
DCHS2
1 1.000 0.080 4 154426241 intron variant A/T snv 0.28 0.810 1.000 2 2012 2016
dbSNP: rs74615166
rs74615166
TRIP4
1 1.000 0.080 15 64433291 intron variant T/C snv 1.6E-02 0.810 1.000 2 2013 2014
dbSNP: rs753129
rs753129 		2 0.925 0.120 4 55802265 downstream gene variant A/G snv 0.23 0.810 1.000 1 2012 2012
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.800 0.882 17 2003 2016
dbSNP: rs6859
rs6859
NECTIN2
10 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 0.800 1.000 13 2008 2019
dbSNP: rs8106922
rs8106922
TOMM40
5 1.000 0.080 19 44898409 intron variant A/G snv 0.36 0.800 1.000 10 2009 2019
dbSNP: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.800 1.000 9 2009 2019
dbSNP: rs10792832
rs10792832 		2 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 0.800 1.000 6 2011 2019
dbSNP: rs440277
rs440277
NECTIN2
2 1.000 0.080 19 44857967 intron variant G/A snv 0.30 0.800 1.000 5 2009 2019