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: rs201921722
rs201921722 		3 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 0.700 1.000 1 2016 2016
dbSNP: rs58598658
rs58598658
KLF12
4 0.925 0.080 13 73887725 intron variant -/A;AA delins 0.700 1.000 1 2017 2017
dbSNP: rs1799752
rs1799752
ACE
25 0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 0.010 1.000 1 2017 2017
dbSNP: rs34177316
rs34177316
APBB2 ; LOC107986273
3 0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 0.700 1.000 1 2016 2016
dbSNP: rs528732638
rs528732638
CHST9 ; AQP4-AS1
5 0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 0.700 1.000 1 2018 2018
dbSNP: rs2522833
rs2522833
PCLO
7 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 0.780 1.000 9 2009 2017
dbSNP: rs242941
rs242941
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
9 0.790 0.200 17 45815154 intron variant A/C snv 0.62 0.030 1.000 3 2007 2013
dbSNP: rs11135349
rs11135349 		1 1.000 0.040 5 165096466 intron variant A/C snv 0.61 0.700 1.000 2 2018 2019
dbSNP: rs2619522
rs2619522
DTNBP1
6 0.827 0.080 6 15653418 intron variant A/C snv 0.26 0.020 1.000 2 2008 2010
dbSNP: rs2715148
rs2715148
PCLO
1 1.000 0.040 7 82820719 3 prime UTR variant A/C snv 0.57 0.800 1.000 2 2009 2011
dbSNP: rs8025231
rs8025231 		1 1.000 0.040 15 37356201 intergenic variant A/C snv 0.48 0.700 1.000 2 2016 2018
dbSNP: rs1039197
rs1039197 		1 1.000 0.040 10 4617005 intergenic variant A/C snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs10904299
rs10904299 		1 1.000 0.040 10 4603975 intergenic variant A/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs11039409
rs11039409
NUP160
2 1.000 0.040 11 47814169 intron variant A/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs11152369
rs11152369
TCF4
5 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs11568817
rs11568817
HTR1B ; LOC105377864
8 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 0.010 1.000 1 2009 2009
dbSNP: rs117235991
rs117235991
APAF1
1 1.000 0.040 12 98699448 missense variant A/C snv 9.5E-03 7.8E-03 0.010 1.000 1 2010 2010
dbSNP: rs1176744
rs1176744
HTR3B
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.010 1.000 1 2008 2008
dbSNP: rs12496634
rs12496634
PBRM1
1 1.000 0.040 3 52675243 intron variant A/C snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs12923444
rs12923444
METTL9
1 1.000 0.040 16 21628389 intron variant A/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1333048
rs1333048
CDKN2B-AS1
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs1343605
rs1343605 		1 1.000 0.040 13 53072913 intergenic variant A/C snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs16854048
rs16854048
BEND4
2 1.000 0.040 4 42121711 intron variant A/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs17673138
rs17673138
NRG1
4 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs184924771
rs184924771
LINC02699
2 1.000 0.040 11 25863658 intergenic variant A/C snv 1.2E-02 0.700 1.000 1 2019 2019