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: rs10524523
rs10524523
TOMM40
7 0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 0.020 1.000 2 2015 2017
dbSNP: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.020 1.000 2 2013 2018
dbSNP: rs17070145
rs17070145
WWC1
10 0.790 0.120 5 168418786 intron variant C/T snv 0.43 0.020 1.000 2 2012 2018
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2016 2016
dbSNP: rs1006737
rs1006737
CACNA1C
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.010 < 0.001 1 2016 2016
dbSNP: rs1018381
rs1018381
DTNBP1
6 0.882 0.040 6 15656839 intron variant G/A snv 0.16 0.010 1.000 1 2009 2009
dbSNP: rs1039049
rs1039049
CFAP299
1 1.000 0.040 4 80416472 intron variant G/A snv 0.98 0.700 1.000 1 2015 2015
dbSNP: rs10521467
rs10521467
PCSK5
2 0.925 0.080 9 76036575 intron variant A/G snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs10748842
rs10748842
NRG3
8 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2020 2020
dbSNP: rs11030108
rs11030108
BDNF ; BDNF-AS
3 1.000 0.040 11 27673917 intron variant A/G snv 0.72 0.010 1.000 1 2013 2013
dbSNP: rs111231532
rs111231532
TTC21A
1 1.000 0.040 3 39135911 intron variant C/T snv 5.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs111600634
rs111600634
LOC105376244
1 1.000 0.040 9 117856347 intron variant T/G snv 1.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs1157659
rs1157659 		2 1.000 0.040 11 27736075 intron variant A/G snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs115881343
rs115881343
TOMM40
2 1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs11637611
rs11637611
PARP6
4 0.851 0.160 15 72259371 intron variant C/T snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs117129097
rs117129097 		1 1.000 0.040 12 128054737 intron variant C/G;T snv 1.9E-03 0.010 1.000 1 2019 2019
dbSNP: rs117529438
rs117529438
LINC02389 ; LINC02231
1 1.000 0.040 12 64979216 intron variant C/T snv 3.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs117605016
rs117605016
TMEM132D
1 1.000 0.040 12 129129840 intron variant C/A snv 9.9E-03 0.700 1.000 1 2015 2015
dbSNP: rs117932393
rs117932393
LINC01505
1 1.000 0.040 9 106390428 intron variant C/T snv 8.4E-03 0.700 1.000 1 2015 2015
dbSNP: rs11887120
rs11887120
DNMT3A
4 0.882 0.080 2 25262866 intron variant C/T snv 0.45 0.010 < 0.001 1 2016 2016
dbSNP: rs12273363
rs12273363
BDNF
11 0.807 0.120 11 27723312 intron variant T/C snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs1256030
rs1256030
ESR2
6 0.827 0.240 14 64280452 intron variant A/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs12628463
rs12628463
HIRA ; C22orf39
1 1.000 0.040 22 19401286 intron variant C/A snv 6.2E-03 0.700 1.000 1 2015 2015
dbSNP: rs13133980
rs13133980
APBB2
1 1.000 0.040 4 41000929 intron variant G/A;C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs13333659
rs13333659
CBFA2T3
2 1.000 0.040 16 88972472 intron variant G/T snv 0.13 0.010 1.000 1 2019 2019