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: rs7815950
rs7815950
SNX31
1 1.000 0.040 8 100646940 intron variant A/G snv 6.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs1336698
rs1336698
FGF14
1 1.000 0.040 13 102211398 intron variant C/T snv 0.85 0.700 1.000 1 2011 2011
dbSNP: rs748910652
rs748910652
NFKB2
1 1.000 0.040 10 102400759 stop gained C/T snv 8.2E-06 0.010 1.000 1 2019 2019
dbSNP: rs2075184
rs2075184 		14 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 0.700 1.000 1 2015 2015
dbSNP: rs62131887
rs62131887 		14 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs11839053
rs11839053 		14 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs9690688
rs9690688
LAMB4 ; LOC105375446
1 1.000 0.040 7 108079717 missense variant C/A snv 8.9E-02 0.17 0.700 1.000 1 2011 2011
dbSNP: rs375099
rs375099
RANBP2
1 1.000 0.040 2 109043821 intergenic variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs6679677
rs6679677
PHTF1
26 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs4246905
rs4246905
TNFSF15
16 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 0.700 1.000 1 2015 2015
dbSNP: rs17140937
rs17140937 		1 1.000 0.040 7 118148430 intergenic variant T/C snv 6.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs62324212
rs62324212
IL21-AS1
15 0.724 0.240 4 122639784 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs7042370
rs7042370
LURAP1L ; LURAP1L-AS1
14 0.724 0.240 9 12785074 intron variant T/C snv 0.58 0.700 1.000 1 2015 2015
dbSNP: rs10988542
rs10988542
FNBP1
14 0.724 0.240 9 129894985 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
IRF1-AS1
14 0.724 0.240 5 132475490 intron variant G/A snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs5977837
rs5977837 		1 1.000 0.040 X 133235903 downstream gene variant T/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11145763
rs11145763
CARD9
14 0.724 0.240 9 136369144 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2807264
rs2807264 		14 0.724 0.240 X 136583619 downstream gene variant C/A snv 0.700 1.000 1 2015 2015
dbSNP: rs12863738
rs12863738 		14 0.724 0.240 X 136949968 intron variant C/T snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs7831697
rs7831697 		14 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs2682665
rs2682665 		1 1.000 0.040 8 13940496 intergenic variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs6649722
rs6649722 		1 1.000 0.040 X 144310656 upstream gene variant C/T snv 4.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs5987017
rs5987017
ATP2B3
1 1.000 0.040 X 153516714 upstream gene variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs10038271
rs10038271
HAVCR1
1 1.000 0.040 5 157043390 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs755374
rs755374 		14 0.724 0.240 5 159402286 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015