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: rs1468326
rs1468326 		1 12 748335 upstream gene variant A/C;T snv 0.040 1.000 4 2005 2018
dbSNP: rs111253292
rs111253292
CORIN
1 4 47661743 missense variant T/G snv 4.6E-03 2.0E-02 0.030 1.000 3 2007 2012
dbSNP: rs1397858410
rs1397858410
CHGA
1 14 92932714 missense variant G/A snv 0.030 1.000 3 2007 2016
dbSNP: rs35929607
rs35929607
STK39
1 2 168179226 intron variant A/G snv 0.27 0.030 0.667 3 2011 2016
dbSNP: rs75770792
rs75770792
CORIN
1 4 47661782 missense variant G/A snv 4.6E-03 2.0E-02 0.030 1.000 3 2007 2012
dbSNP: rs11105378
rs11105378
ATP2B1
1 12 89696964 intron variant C/T snv 0.15 0.020 1.000 2 2010 2012
dbSNP: rs200339834
rs200339834
RGS2
1 1 192810186 missense variant G/A snv 1.2E-04 7.0E-05 0.020 1.000 2 2005 2008
dbSNP: rs2070759
rs2070759
ATP2B1
1 12 89623959 intron variant G/T snv 0.49 0.020 1.000 2 2010 2016
dbSNP: rs4305
rs4305
ACE
1 17 63480868 intron variant A/G snv 0.45 0.020 1.000 2 2011 2013
dbSNP: rs10033366
rs10033366
ENPEP
1 4 110409934 intron variant T/C snv 0.92 0.700 1.000 1 2018 2018
dbSNP: rs10069554
rs10069554 		1 5 33204354 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10086846
rs10086846
CYP11B2 ; GML
1 8 142915715 intron variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs10188442
rs10188442
GPR39
1 2 132431666 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011
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: 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: 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