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: rs13440581
rs13440581
GPR50
5 0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 0.010 1.000 1 2015 2015
dbSNP: rs1368748
rs1368748
CADM2
1 1.000 0.040 3 85363180 intron variant A/G snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs1390938
rs1390938
SLC18A1
7 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 0.010 1.000 1 2016 2016
dbSNP: rs1401663578
rs1401663578
ACE
4 0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 0.010 1.000 1 2017 2017
dbSNP: rs17196295
rs17196295
SATB2
1 1.000 0.040 2 199287475 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs2071559
rs2071559
KDR
26 0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 0.010 1.000 1 2019 2019
dbSNP: rs2478813
rs2478813
PLXNA2
4 0.882 0.080 1 208073865 intron variant A/G snv 0.85 0.010 1.000 1 2007 2007
dbSNP: rs28639817
rs28639817
SGCZ
1 1.000 0.040 8 14293898 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2941026
rs2941026
CCKBR
2 1.000 0.040 11 6261042 intron variant A/G snv 0.51 0.010 1.000 1 2017 2017
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.010 1.000 1 2016 2016
dbSNP: rs391236
rs391236 		1 1.000 0.040 5 103342372 intergenic variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs3988211
rs3988211
WBP2
1 1.000 0.040 17 75850024 intron variant A/G snv 0.95 0.700 1.000 1 2018 2018
dbSNP: rs4434138
rs4434138
STAB1
2 1.000 0.040 3 52522874 missense variant A/G snv 8.0E-06; 0.44 0.39 0.700 1.000 1 2018 2018
dbSNP: rs4813627
rs4813627 		2 1.000 0.040 20 3074867 downstream gene variant A/G snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs5742905
rs5742905
CBS
22 0.701 0.360 21 43063074 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs589092
rs589092
PCCB
1 1.000 0.040 3 136260856 intron variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs61734645
rs61734645
DNAH1
1 1.000 0.040 3 52349827 intron variant A/G snv 4.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs6269
rs6269
COMT ; MIR4761
10 0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 0.010 1.000 1 2019 2019
dbSNP: rs75012854
rs75012854
COMT ; MIR4761
5 0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs774847933
rs774847933
COMT ; MIR4761
5 0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs78260322
rs78260322
RNF103-CHMP3 ; LOC105374845
1 1.000 0.040 2 86566075 intron variant A/G snv 7.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs80533
rs80533 		2 1.000 0.040 22 40689965 intergenic variant A/G snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs900418273
rs900418273
ANKK1
8 0.807 0.120 11 113393764 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs9296158
rs9296158
FKBP5 ; LOC112267956
16 0.763 0.080 6 35599305 intron variant A/G snv 0.65 0.010 1.000 1 2012 2012
dbSNP: rs9340799
rs9340799
ESR1
62 0.583 0.680 6 151842246 intron variant A/G snv 0.32 0.010 1.000 1 2012 2012