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: rs9988642
rs9988642
IL23R
3 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 0.800 1.000 1 2012 2012
dbSNP: rs1001007
rs1001007
CCR5AS
5 0.827 0.120 3 46387167 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
IRF1-AS1 ; LINC02863
5 0.827 0.120 5 132421409 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10088247
rs10088247
CSMD1
1 1.000 0.040 8 3826677 intron variant C/T snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs10094579
rs10094579 		6 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs10405308
rs10405308 		1 1.000 0.040 19 1312729 intergenic variant G/A snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs1042636
rs1042636
CASR
23 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
11 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs10510607
rs10510607
CMC1
5 0.827 0.120 3 28244770 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs10515778
rs10515778
LINC01932
1 1.000 0.040 5 159231004 intron variant A/G snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs1051738
rs1051738
PDE4A
1 1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 0.700 1.000 1 2015 2015
dbSNP: rs10743181
rs10743181 		5 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781 		11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs10750899
rs10750899 		5 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 0.700 1.000 1 2016 2016
dbSNP: rs10758669
rs10758669 		10 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
5 0.827 0.120 10 62594503 intron variant C/T snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10775412
rs10775412
KSR1
5 0.827 0.120 17 27542007 intron variant A/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs10789285
rs10789285 		2 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10800314
rs10800314 		5 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs10822050
rs10822050 		14 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10870077
rs10870077
CARD9
5 0.827 0.120 9 136369439 intron variant C/G snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10888501
rs10888501
LCE3E
1 1.000 0.040 1 152565478 downstream gene variant G/A snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs10889676
rs10889676
IL23R
5 0.827 0.120 1 67256884 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10960680
rs10960680 		1 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs10988542
rs10988542
FNBP1
14 0.724 0.240 9 129894985 intron variant G/A;C snv 0.700 1.000 1 2015 2015