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: rs11076962
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11076962
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs11077204
rs11077204
RBFOX1
16 7617185 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs11077207
rs11077207
RBFOX1
16 7618478 intron variant C/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs11642387
rs11642387
RBFOX1
16 6703238 intron variant A/G snv 6.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11643447
rs11643447
RBFOX1
16 6649260 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs11645781
rs11645781
RBFOX1
16 6846127 intron variant A/C;G;T snv
CUI: C0018810
Disease: heart rate
heart rate 		0.800 1.000 1 2013 2013
dbSNP: rs11646221
rs11646221
RBFOX1
16 7616086 intron variant G/T snv 0.47
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs11865256
rs11865256
RBFOX1
16 7215069 intron variant C/T snv 0.38
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs12709186
rs12709186
RBFOX1
16 7199471 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs12933772
rs12933772
RBFOX1
16 6510429 intron variant C/G snv 0.23
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs17143122
rs17143122
RBFOX1
16 7259990 intron variant C/T snv 1.8E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.700 1.000 1 2016 2016
dbSNP: rs2058527
rs2058527
RBFOX1
16 6654748 intron variant T/G snv 0.75
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3095508
rs3095508
RBFOX1
16 6500399 intron variant C/A;G;T snv
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs35450617
rs35450617
RBFOX1
16 6839674 intron variant T/G snv 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs3785229
rs3785229
RBFOX1
16 7620997 intron variant A/G snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3785238
rs3785238
RBFOX1
16 7615555 intron variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs4786084
rs4786084
RBFOX1
16 6122772 intron variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs7186834
rs7186834
RBFOX1
16 7623253 intron variant T/C snv 0.51
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs7194617
rs7194617
RBFOX1
16 7418351 intron variant T/A snv 0.62
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7206841
rs7206841
RBFOX1
16 6531745 intron variant G/A;C;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs77684884
rs77684884
RBFOX1
16 6449119 intron variant A/G snv 0.13
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs8044082
rs8044082
RBFOX1
16 6553020 intron variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs8061082
rs8061082
RBFOX1
16 6704527 non coding transcript exon variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs870288
rs870288
RBFOX1
16 5535851 intron variant A/G snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012