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: rs7638018
rs7638018
TF
1.000 0.040 3 133776617 intron variant A/G snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs7646118
rs7646118
TF ; INHCAP
3 133731195 intron variant C/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177178
rs8177178
TF ; INHCAP
0.925 0.080 3 133744428 intron variant G/A snv 0.33
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177191
rs8177191
TF ; INHCAP
3 133749295 intron variant G/A snv 0.13
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177197
rs8177197
TF ; INHCAP
3 133750686 intron variant G/A snv 0.27
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177213
rs8177213
TF ; INHCAP
3 133753383 intron variant A/C snv 0.25
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177220
rs8177220
TF
3 133754781 intron variant G/C;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177233
rs8177233
TF
1.000 0.080 3 133757117 intron variant A/G snv 6.9E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs8177240
rs8177240
TF
3 133758857 intron variant T/C;G snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177252
rs8177252
TF
3 133761330 non coding transcript exon variant C/A;G snv 0.31
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177272
rs8177272
TF
1.000 0.040 3 133764026 intron variant G/A snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177313
rs8177313
TF ; INHCAP
3 133745258 intron variant T/A;G snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs9830001
rs9830001
TF ; INHCAP
3 133714626 intron variant G/A;C snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs9843728
rs9843728
TF ; SRPRB
3 133782563 3 prime UTR variant C/A;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8177318
rs8177318
TF ; INHCAP
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1799899
rs1799899
TF
1.000 0.080 3 133756968 missense variant G/A snv 5.2E-02 4.5E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 1.000 1 2011 2011
dbSNP: rs1799852
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs1049296
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 1.000 1 2011 2011