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: 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: rs1041536
rs1041536 		1 1.000 0.040 20 9907627 intergenic variant T/C snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs10447760
rs10447760 		4 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 0.010 < 0.001 1 2019 2019
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: rs112961612
rs112961612 		1 1.000 0.040 20 41872026 intergenic variant T/A snv 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs113793030
rs113793030 		1 1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs115199861
rs115199861
PFN1P1
1 1.000 0.040 1 171670879 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs115700680
rs115700680 		1 1.000 0.040 1 171381070 intergenic variant T/G snv 1.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs115764752
rs115764752
LOC105371614
1 1.000 0.040 1 171778066 upstream gene variant T/C snv 7.9E-03 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: rs116065238
rs116065238 		1 1.000 0.040 1 171482283 upstream gene variant A/G snv 4.3E-03 0.700 1.000 1 2015 2015
dbSNP: rs116237496
rs116237496 		1 1.000 0.040 8 101033687 upstream gene variant T/C snv 4.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs117070989
rs117070989 		1 1.000 0.040 6 137490510 downstream gene variant C/A snv 8.3E-03 0.700 1.000 1 2015 2015
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: rs117224174
rs117224174 		1 1.000 0.040 6 114654261 intergenic variant G/A snv 2.2E-02 0.700 1.000 1 2015 2015
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: rs1187120
rs1187120 		3 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 0.010 1.000 1 2015 2015
dbSNP: rs1216578110
rs1216578110
APP
1 1.000 0.040 21 25955652 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs12230170
rs12230170 		1 1.000 0.040 12 128762838 intergenic variant T/A;G snv 0.700 1.000 1 2015 2015