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: rs12716850
rs12716850
WWOX
16 78154006 intron variant A/C;G snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.800 1.000 1 2012 2012
dbSNP: rs8056446
rs8056446
WWOX
16 78154599 intron variant G/A;C snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.800 1.000 1 2012 2012
dbSNP: rs9923451
rs9923451
WWOX
1.000 0.080 16 78918542 intron variant A/C;G snv
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2011 2011
dbSNP: rs2345443
rs2345443
WWOX
16 78191736 intron variant A/C;G snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs1079572
rs1079572
WWOX
16 78153241 intron variant G/A snv 0.57
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2014 2014
dbSNP: rs1110544
rs1110544
WWOX
16 79165213 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs113496184
rs113496184
WWOX
16 79006207 intron variant G/C;T snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs113496184
rs113496184
WWOX
16 79006207 intron variant G/C;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs12149527
rs12149527
WWOX
1.000 0.080 16 79076699 intron variant C/T snv 0.36
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs12445943
rs12445943
WWOX
16 78775175 intron variant G/A snv 0.17
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.700 1.000 1 2016 2016
dbSNP: rs12449066
rs12449066
WWOX
16 79143396 intron variant A/C;G snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs12716850
rs12716850
WWOX
16 78154006 intron variant A/C;G snv
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2012 2012
dbSNP: rs12716852
rs12716852
WWOX
16 78154841 intron variant G/A snv 0.57
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2011 2011
dbSNP: rs12716852
rs12716852
WWOX
16 78154841 intron variant G/A snv 0.57
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2011 2011
dbSNP: rs16944118
rs16944118
WWOX
16 78773946 intron variant G/A snv 0.14
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.700 1.000 1 2016 2016
dbSNP: rs17706989
rs17706989
WWOX
16 78536060 intron variant C/G snv 2.6E-02
CUI: C0684328
Disease: Reasoning
Reasoning 		0.700 1.000 1 2011 2011
dbSNP: rs1875939
rs1875939
WWOX
16 78977175 intron variant G/C snv 0.95
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs1912804
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2017 2017