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: 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: 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: 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: 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: 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: rs2078543
rs2078543
CASC15
6 21996631 intron variant A/G snv 0.69
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2012 2012
dbSNP: rs2744132
rs2744132
CASC15 ; LOC105374971
6 22392594 intron variant G/A snv 0.14
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2744133
rs2744133
CASC15 ; LOC105374971
6 22392031 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs3736675
rs3736675
CASC15
6 22110919 splice region variant G/A snv 3.0E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs67258057
rs67258057
CASC15
6 21948833 intron variant G/A snv 4.8E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs6903716
rs6903716
CASC15
6 21956173 intron variant A/G snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs6926491
rs6926491
CASC15
6 21724439 intron variant G/A snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs6934973
rs6934973
CASC15
6 21920795 intron variant A/G snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs74360995
rs74360995
CASC15
6 21886258 non coding transcript exon variant T/C snv 0.12
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7760082
rs7760082
CASC15
6 21919156 intron variant G/A snv 0.59
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019