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: 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
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: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 1.000 1 2011 2011
dbSNP: rs10935073
rs10935073
TF ; INHCAP
3 133720340 intron variant T/C snv 0.34
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs11921527
rs11921527
TF ; INHCAP
3 133722323 intron variant G/A;C snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs12639304
rs12639304
TF ; INHCAP
3 133722750 intron variant A/T snv 0.42
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs1358024
rs1358024
TF
3 133765344 intron variant C/T snv 0.13
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs1525889
rs1525889
TF
3 133771189 intron variant A/C snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs1525892
rs1525892
TF
1.000 0.040 3 133765868 intron variant G/A;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 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: rs1800277
rs1800277
TF ; INHCAP
3 133747311 intron variant C/T snv 7.0E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs1830084
rs1830084
TF ; SRPRB ; LOC105374116
0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs2692695
rs2692695
TF
1.000 0.080 3 133766610 intron variant A/G snv 0.56
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0337439
Disease: Iron measurement
Iron measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31
CUI: C0428578
Disease: Iron level result
Iron level result 		0.700 1.000 1 2011 2011
dbSNP: rs41295800
rs41295800
TF
3 133765869 intron variant T/-;TT delins
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs4459901
rs4459901
TF ; INHCAP
3 133746855 intron variant T/C snv 0.35
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs4525863
rs4525863
TF ; INHCAP
1.000 0.080 3 133717292 intron variant C/A snv 0.32
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs4854760
rs4854760
TF
3 133779897 3 prime UTR variant A/G snv 0.35
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs4854761
rs4854761
TF
3 133779945 3 prime UTR variant G/A snv 0.33
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs4854762
rs4854762
TF
3 133780219 3 prime UTR variant G/A;C snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs6439431
rs6439431
TF ; INHCAP
3 133729265 intron variant A/C snv 0.38
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs6774822
rs6774822
TF ; INHCAP
3 133723168 intron variant G/C;T snv 0.41
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs6775042
rs6775042
TF ; INHCAP
3 133723401 intron variant G/C;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011
dbSNP: rs6782523
rs6782523
TF ; INHCAP
3 133720073 intron variant C/G;T snv 0.34
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2011 2011