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: rs10255208
rs10255208 		2 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 0.010 1.000 1 2019 2019
dbSNP: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2014 2014
dbSNP: rs1056534
rs1056534
TBCD ; FN3K
5 0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs1063537
rs1063537
ADIPOQ ; ADIPOQ-AS1
6 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs10770125
rs10770125
IGF2 ; IGF2-AS ; INS-IGF2
4 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 0.010 1.000 1 2013 2013
dbSNP: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs10951509
rs10951509
ELMO1
1 1.000 0.120 7 37173878 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs11130362
rs11130362
TKT
1 1.000 0.120 3 53231750 non coding transcript exon variant C/T snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs1129456
rs1129456
GREM1
1 1.000 0.120 15 32734466 3 prime UTR variant A/T snv 0.19 0.010 1.000 1 2010 2010
dbSNP: rs1136410
rs1136410
PARP1
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
dbSNP: rs1137933
rs1137933
NOS2
4 0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 0.010 1.000 1 2016 2016
dbSNP: rs1143770
rs1143770
MIR100HG ; MIRLET7A2
4 0.882 0.200 11 122146890 intron variant C/T snv 0.53 0.010 1.000 1 2013 2013
dbSNP: rs11538209
rs11538209
ALB
2 1.000 0.120 4 73404356 missense variant T/C snv 0.010 < 0.001 1 2001 2001
dbSNP: rs1157043147
rs1157043147
ACE
1 1.000 0.120 17 63477150 missense variant T/C snv 2.8E-05 0.010 1.000 1 2003 2003
dbSNP: rs11645214
rs11645214
SF3B3
1 1.000 0.120 16 70575084 3 prime UTR variant A/G snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs11646213
rs11646213 		6 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 0.010 1.000 1 2017 2017
dbSNP: rs11651270
rs11651270
NLRP1
4 0.882 0.240 17 5521757 missense variant T/C snv 0.45 0.47 0.010 1.000 1 2018 2018
dbSNP: rs11771443
rs11771443
NOS3
8 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs1177506410
rs1177506410
AGT
12 0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs11886047
rs11886047 		1 1.000 0.120 2 43623451 upstream gene variant T/A;C snv 0.20 0.010 1.000 1 2008 2008
dbSNP: rs11887534
rs11887534
ABCG5 ; ABCG8
29 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 0.010 1.000 1 2015 2015
dbSNP: rs11915160
rs11915160
SOX2 ; SOX2-OT
5 0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 0.010 1.000 1 2010 2010
dbSNP: rs12449782
rs12449782 		3 0.925 0.200 17 63498888 intron variant G/A snv 0.41 0.010 1.000 1 2007 2007
dbSNP: rs1252906
rs1252906
DAAM1
1 1.000 0.120 14 59192073 intron variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs1253192
rs1253192 		1 1.000 0.120 14 59376688 intergenic variant A/G snv 0.92 0.010 1.000 1 2013 2013