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: rs10506346
rs10506346 		1 12 56937074 upstream gene variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs10788639
rs10788639
TSPAN14
1 10 80473469 intron variant C/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs10902094
rs10902094 		1 11 1119225 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10965935
rs10965935
LOC101929563
1 9 23581213 intron variant C/G;T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10975277
rs10975277
RIC1 ; ERMP1
1 9 5774661 3 prime UTR variant G/A;C snv 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 1 2019 2019
dbSNP: rs111782388
rs111782388
ITK
1 5 157202838 intron variant C/T snv 6.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs11178649
rs11178649
TSPAN8
1 12 71139458 intron variant G/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs112068732
rs112068732 		1 17 40204213 regulatory region variant A/G snv 3.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs112119265
rs112119265
CARD11
1 7 3022995 intron variant T/G snv 5.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs112204664
rs112204664
CASC15
1 6 21867474 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs112401631
rs112401631 		8 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs11255938
rs11255938 		1 10 8808772 intergenic variant C/T snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs113660049
rs113660049 		1 19 9026584 intergenic variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11495981
rs11495981
JAZF1
2 1.000 0.120 7 28137682 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs115008099
rs115008099
IL13 ; TH2LCRR
2 1.000 0.080 5 132656189 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs11567694
rs11567694
IL7R ; LOC105374724
1 5 35857602 intron variant A/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs11715524
rs11715524
TFRC
3 0.925 0.080 3 196035621 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs117552144
rs117552144
GNA15
1 19 3136093 5 prime UTR variant C/T snv 3.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs117710327
rs117710327 		5 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs12123821
rs12123821
FLG-AS1 ; LOC112268240
4 0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs12190426
rs12190426
AHI1
1 6 135391300 intron variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs12365699
rs12365699 		5 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs12655443
rs12655443
LOC105378204
2 1.000 0.080 5 142088291 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019