Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10775354
rs10775354
1.000 0.080 16 6757689 intron variant A/C;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10780661
rs10780661
1.000 0.080 9 84311392 intron variant A/G;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs1086603
rs1086603
0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10894993
rs10894993
0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10918931
rs10918931
1.000 0.080 1 168592853 intergenic variant T/C snv 0.61
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10944489
rs10944489
1.000 0.080 6 90554374 intron variant G/A snv 3.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10947261
rs10947261
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10956273
rs10956273
1.000 0.080 8 125953914 non coding transcript exon variant A/G snv 6.9E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10974284
rs10974284
1.000 0.080 9 4028700 intron variant T/C snv 1.2E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11030600
rs11030600
1.000 0.080 11 29174695 intron variant T/G snv 8.9E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs1105358
rs1105358
1.000 0.080 9 16265821 intron variant G/C snv 0.10
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11081843
rs11081843
1.000 0.080 18 34103632 intron variant T/C snv 0.16
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11083572
rs11083572
1.000 0.080 19 28604968 intron variant T/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11165851
rs11165851
1.000 0.080 1 97380021 intron variant T/A snv 0.93
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11189017
rs11189017
1.000 0.080 10 81258621 intergenic variant T/G snv 1.0E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11206948
rs11206948
1.000 0.080 1 56984813 intron variant T/C snv 3.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11210604
rs11210604
0.925 0.080 1 42158001 downstream gene variant T/A;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11221067
rs11221067
1.000 0.080 11 127823799 intergenic variant C/T snv 8.8E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11238999
rs11238999
1.000 0.080 10 44345031 regulatory region variant G/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11574049
rs11574049
VDR
1.000 0.080 12 47878732 intron variant A/G snv 1.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11603020
rs11603020
0.925 0.120 11 57606859 intron variant T/C snv 0.21
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11604865
rs11604865
1.000 0.080 11 40636452 intron variant T/C snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs1163521
rs1163521
1.000 0.080 1 105786097 intergenic variant T/A;C;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11687856
rs11687856
1.000 0.080 2 31117780 intron variant G/A snv 0.19
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs11697253
rs11697253
1.000 0.080 20 25014378 intron variant A/G snv 9.9E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009