Source: GWASCAT

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: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.800 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 1 2012 2012
dbSNP: rs10502861
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 1 2016 2016
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 1 2016 2016
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 1 2016 2016
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2016 2016
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 1 2016 2016
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs34800162
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 1 2016 2016
dbSNP: rs8090126
rs8090126
SLC14A2
18 45231762 intron variant T/C snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 1 2017 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.800 1.000 1 2012 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 1 2017 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 1 2017 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs8085664
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs9807668
rs9807668
SLC14A2
18 45247933 intron variant C/T snv 6.9E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs9807668
rs9807668
SLC14A2
18 45247933 intron variant C/T snv 6.9E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs11082438
rs11082438
SLC14A2
1.000 0.120 18 45285245 intron variant G/T snv 8.3E-02
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		0.700 1.000 1 2014 2014