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
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: rs2243803
rs2243803
18 45376707 intron variant T/A snv 0.53
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs7227483
rs7227483
18 45607165 intron variant A/G;T snv
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.800 1.000 1 2012 2012
dbSNP: rs8085664
rs8085664
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: rs10438964
rs10438964
18 45370664 intron variant C/T snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs10502861
rs10502861
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
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
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
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
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
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: rs11082438
rs11082438
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
dbSNP: rs1484873
rs1484873
18 45627020 missense variant A/C;G snv 0.91
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019
dbSNP: rs16978350
rs16978350
18 45360534 intron variant G/A;C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2193635
rs2193635
18 45516271 intron variant C/T snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs2543029
rs2543029
18 45518310 intron variant C/A snv 0.74
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2019 2019
dbSNP: rs2612539
rs2612539
0.925 0.040 18 45497596 intron variant G/A;C snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs2612539
rs2612539
0.925 0.040 18 45497596 intron variant G/A;C snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs2705366
rs2705366
18 45534827 intron variant A/G snv 0.23
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs34800162
rs34800162
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
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
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
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
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
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