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: rs6939340
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.840 1.000 1 2008 2017
dbSNP: rs4712653
rs4712653
CASC15
0.882 0.080 6 22125735 intron variant T/C;G snv
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.830 1.000 2 2008 2017
dbSNP: rs9295536
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.830 1.000 1 2008 2017
dbSNP: rs4712652
rs4712652
CASC15
1.000 0.080 6 22078386 intron variant G/A snv 0.64
CUI: C0028754
Disease: Obesity
Obesity 		0.720 1.000 1 2009 2013
dbSNP: rs113760175
rs113760175
CASC15
6 22343363 intron variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs1928168
rs1928168
CASC15
6 22017509 intron variant T/C snv 0.36
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 2 2011 2012
dbSNP: rs6909752
rs6909752
CASC15
1.000 0.040 6 22612400 intron variant G/A snv 0.35
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2017 2018
dbSNP: rs6911827
rs6911827
CASC15
6 22130372 intron variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2017 2019
dbSNP: rs10484389
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02
CUI: C0019158
Disease: Hepatitis
Hepatitis 		0.700 1.000 1 2014 2014
dbSNP: rs10946507
rs10946507
CASC15
1.000 0.040 6 22100138 intron variant G/A;T snv
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.700 1.000 1 2018 2018
dbSNP: rs112204664
rs112204664
CASC15
6 21867474 intron variant G/A snv 0.13
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs113760175
rs113760175
CASC15
6 22343363 intron variant G/A;T snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs113760175
rs113760175
CASC15
6 22343363 intron variant G/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs113977268
rs113977268
CASC15 ; LOC105374971
6 22359286 intron variant G/A snv 5.7E-02
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs113977268
rs113977268
CASC15 ; LOC105374971
6 22359286 intron variant G/A snv 5.7E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1205896
rs1205896
CASC15
6 22341240 intron variant G/A snv 0.47
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs12196123
rs12196123
CASC15
1.000 0.040 6 22082034 intron variant C/T snv 0.47
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.700 1.000 1 2018 2018
dbSNP: rs12212674
rs12212674
CASC15
1.000 0.040 6 22086845 intron variant T/A snv 0.48
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.700 1.000 1 2015 2015
dbSNP: rs12525417
rs12525417
CASC15
6 22591478 intron variant C/T snv 0.33
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs13198081
rs13198081
CASC15
6 22017314 intron variant G/C snv 0.35
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs13198656
rs13198656
CASC15
1.000 0.040 6 22004680 intron variant C/A;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs141007801
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs141007801
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs1928175
rs1928175
CASC15
6 22079256 intron variant G/A snv 0.55
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs196052
rs196052
CASC15
1.000 0.040 6 22056971 intron variant T/A;C snv
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		0.700 1.000 1 2018 2018