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: rs10036789
rs10036789 		3 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10044254
rs10044254
FBXL7
2 0.925 0.080 5 15783487 intron variant A/G snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs10158467
rs10158467 		2 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10175070
rs10175070
CCL20
1 1.000 0.080 2 227805859 5 prime UTR variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10187276
rs10187276 		2 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs10208293
rs10208293
IL18R1 ; IL1RL1
4 0.882 0.160 2 102349850 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10414065
rs10414065 		4 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2013 2016
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs10445308
rs10445308
IKZF3
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs10494132
rs10494132
CHIA
4 0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs10519031
rs10519031 		1 1.000 0.080 15 59890806 regulatory region variant T/C snv 2.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.010 1.000 1 2013 2013
dbSNP: rs10774625
rs10774625
ATXN2
13 0.763 0.320 12 111472415 intron variant A/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs10830123
rs10830123
NPS
1 1.000 0.080 10 127551386 intron variant G/C snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs10836538
rs10836538
PRR5L
2 0.925 0.080 11 36343703 intron variant G/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs10924993
rs10924993 		2 0.925 0.080 1 236296485 intergenic variant T/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs10995245
rs10995245
ZNF365 ; LOC105378327
3 0.882 0.160 10 62631615 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11000019
rs11000019
PSAP
1 1.000 0.080 10 71831773 intron variant G/A snv 3.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs11021111
rs11021111 		1 1.000 0.080 11 95270099 intergenic variant C/G snv 4.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs1102705
rs1102705 		3 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 0.700 1.000 1 2019 2019
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11071559
rs11071559
RORA
4 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.700 1.000 2 2019 2019
dbSNP: rs1117490
rs1117490
TRIM26
2 0.925 0.080 6 30202733 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs11178648
rs11178648
TSPAN8
2 0.925 0.080 12 71139430 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019