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: rs10809520
rs10809520 		2 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs10811965
rs10811965
ELAVL2
1 1.000 0.040 9 23741280 intron variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10817969
rs10817969
ASTN2
1 1.000 0.040 9 116968766 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10830220
rs10830220
LOC107984363
1 1.000 0.040 11 89140984 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10835210
rs10835210
BDNF ; BDNF-AS
4 0.882 0.040 11 27674363 intron variant C/A;G snv 0.010 1.000 1 2009 2009
dbSNP: rs10865974
rs10865974
GNL3 ; PBRM1
2 0.925 0.040 3 52684264 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10877887
rs10877887
LINC01465 ; MIRLET7I
18 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 0.010 1.000 1 2015 2015
dbSNP: rs10884216
rs10884216
LINC02627
2 0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs10890020
rs10890020
LOC105378800
1 1.000 0.040 1 73203153 intergenic variant A/G snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10890045
rs10890045 		1 1.000 0.040 1 73531941 intergenic variant T/C snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs10891564
rs10891564 		2 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs10896636
rs10896636
ZDHHC5
1 1.000 0.040 11 57680560 intron variant C/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10904290
rs10904290 		1 1.000 0.040 10 4574670 intergenic variant A/G snv 8.4E-02 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: rs10904300
rs10904300 		1 1.000 0.040 10 4606242 intergenic variant T/C snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs10904319
rs10904319 		1 1.000 0.040 10 4699650 intergenic variant T/C snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs10904321
rs10904321
LOC107984197
1 1.000 0.040 10 4704153 TF binding site variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10904323
rs10904323
LOC105376375 ; LOC107984197
1 1.000 0.040 10 4706048 regulatory region variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10904328
rs10904328
LOC105376375
1 1.000 0.040 10 4730412 intergenic variant G/A snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10904332
rs10904332
LOC105376375
1 1.000 0.040 10 4746246 downstream gene variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10904333
rs10904333
LOC105376375
1 1.000 0.040 10 4750385 intron variant T/C snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs10913112
rs10913112
COP1
1 1.000 0.040 1 175944692 downstream gene variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10914456
rs10914456
HCRTR1
2 1.000 0.040 1 31622570 intron variant T/C snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs10922744
rs10922744
ZNF326
1 1.000 0.040 1 90027467 synonymous variant G/A snv 0.61; 1.2E-05 0.57 0.010 1.000 1 2012 2012
dbSNP: rs10929355
rs10929355
NBAS
1 1.000 0.040 2 15258840 intron variant T/G snv 0.56 0.700 1.000 1 2018 2018