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: rs10184428
rs10184428 		5 2 164155317 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10188442
rs10188442
GPR39
1 2 132431666 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1027989
rs1027989
LYN
3 8 55901862 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10279895
rs10279895 		1 7 27288591 intergenic variant A/G snv 2.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs1042039
rs1042039
XDH
1 2 31335440 3 prime UTR variant T/C snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs1042309696
rs1042309696
ACE
2 17 63487006 synonymous variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs10491093
rs10491093 		1 17 10978681 intergenic variant T/G snv 0.72 0.010 1.000 1 2008 2008
dbSNP: rs10491334
rs10491334
CAMK4
1 5 111436706 intron variant C/T snv 0.14 0.010 1.000 1 2016 2016
dbSNP: rs10496288
rs10496288 		1 2 83065441 intergenic variant T/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10496289
rs10496289 		1 2 83066256 intergenic variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10509676
rs10509676
CYP2C19
1 10 94763288 intron variant A/G;T snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs10519963
rs10519963
NR3C2
1 4 148376523 intron variant G/A snv 0.12 0.010 1.000 1 2011 2011
dbSNP: rs10520097
rs10520097
LPIN1
1 2 11793260 intron variant A/G snv 0.12 0.010 1.000 1 2008 2008
dbSNP: rs1054889
rs1054889
XDH
1 2 31334442 3 prime UTR variant G/A snv 0.40 0.010 1.000 1 2015 2015
dbSNP: rs1058261
rs1058261
DES
2 2 219420587 synonymous variant C/T snv 0.33 0.37 0.010 < 0.001 1 2018 2018
dbSNP: rs1061376
rs1061376
FBLN2
1 3 13637835 missense variant C/G;T snv 0.37 0.41 0.010 1.000 1 2012 2012
dbSNP: rs10737175
rs10737175 		1 1 159750152 intergenic variant T/C snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs10738554
rs10738554
SLC24A2
1 9 19904105 intergenic variant T/C snv 0.46 0.010 1.000 1 2017 2017
dbSNP: rs10745332
rs10745332
CAPZA1
3 1 112646431 intron variant G/A snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs10776752
rs10776752
WNT2B
4 1 112501706 intron variant G/T snv 8.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs1078499
rs1078499
AGT
1 1 230713350 intron variant A/G snv 0.30 0.010 1.000 1 2016 2016
dbSNP: rs10785581
rs10785581
LOC105369743
1 12 45537190 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10792367
rs10792367
SLC22A8
1 11 62991327 non coding transcript exon variant C/G snv 0.44 0.010 < 0.001 1 2011 2011
dbSNP: rs10794501
rs10794501
FCN3
1 1 27372958 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs10860812
rs10860812
DRAM1
1 12 101894592 intron variant G/A snv 0.59 0.010 1.000 1 2013 2013