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: rs10438964
rs10438964
SLC14A2
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: rs1484873
rs1484873
SLC14A2
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
SLC14A2
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
SLC14A2
18 45516271 intron variant C/T snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs2243803
rs2243803
SLC14A2
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: rs2543029
rs2543029
SLC14A2
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: rs2705366
rs2705366
SLC14A2
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: rs4890293
rs4890293
SLC14A2
18 45632973 intron variant A/G snv 0.92
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4890568
rs4890568
SLC14A2 ; LOC105372093
18 45651657 intron variant G/A snv 0.93
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2010 2010
dbSNP: rs7227483
rs7227483
SLC14A2 ; LOC107985153
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: rs7232775
rs7232775
SLC14A2
18 45622439 intron variant C/T snv 0.76
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2011 2011
dbSNP: rs7236548
rs7236548
SLC14A2
18 45517785 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
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: rs8093563
rs8093563
SLC14A2
18 45299752 intron variant G/A snv 0.32
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
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: rs2612539
rs2612539
SLC14A2 ; SLC14A2-AS1
0.925 0.040 18 45497596 intron variant G/A;C snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2612539
rs2612539
SLC14A2 ; SLC14A2-AS1
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: 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