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: rs10160659
rs10160659
1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs17044542
rs17044542
1.000 0.080 3 6299812 intron variant A/C snv 5.2E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs2647046
rs2647046
0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs2839750
rs2839750
1.000 0.080 2 52901952 intron variant A/C snv 3.1E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs2858884
rs2858884
0.925 0.200 6 32732306 upstream gene variant A/C snv 0.23
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.800 1.000 1 2010 2010
dbSNP: rs7175718
rs7175718
0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs7187262
rs7187262
1.000 0.080 16 69460376 intron variant A/C snv 0.11
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs7579759
rs7579759
1.000 0.080 2 28470781 intron variant A/C snv 0.42
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs9270986
rs9270986
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs9373298
rs9373298
1.000 0.080 6 141198693 regulatory region variant A/C snv 0.27
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10226621
rs10226621
1.000 0.080 7 4068008 intron variant A/C;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs17138435
rs17138435
0.882 0.120 11 79481943 TF binding site variant A/C;G snv 1.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs686881
rs686881
1.000 0.080 18 54287164 intron variant A/C;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs7105164
rs7105164
1.000 0.080 11 12132546 intron variant A/C;G snv 5.0E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs6023560
rs6023560
0.882 0.120 20 54743554 intergenic variant A/C;G;T snv 0.12
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
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: rs539703
rs539703
0.882 0.200 6 32320685 intron variant A/C;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs9267954
rs9267954
0.882 0.200 6 32245275 regulatory region variant A/C;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10091183
rs10091183
1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs1009449
rs1009449
1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03
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: 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: 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
dbSNP: rs1201324
rs1201324
1.000 0.080 13 89601725 intron variant A/G snv 0.98
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs12695894
rs12695894
0.882 0.120 3 148724853 intron variant A/G snv 2.7E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009