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: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2016 2018
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs201462698
rs201462698
SIK3
1.000 0.080 11 116897884 intron variant AA/-;A;AAA delins 8.4E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs11216183
rs11216183
SIK3
11 116910829 intron variant C/A snv 0.10
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs11216183
rs11216183
SIK3
11 116910829 intron variant C/A snv 0.10
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs11216183
rs11216183
SIK3
11 116910829 intron variant C/A snv 0.10
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs12099358
rs12099358
SIK3 ; APOA1-AS
11 116855332 non coding transcript exon variant C/A snv 0.24
CUI: C0523522
Disease: beta-Endorphin measurement
beta-Endorphin measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1076485
rs1076485
SIK3
11 116901725 intron variant C/T snv 0.22
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11216230
rs11216230
SIK3
11 117014073 intron variant G/A snv 3.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2014 2019
dbSNP: rs139961185
rs139961185
SIK3
11 116936627 intron variant G/A snv 1.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2014 2019
dbSNP: rs11827828
rs11827828
SIK3
1.000 0.040 11 116884868 intron variant G/A snv 0.16
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018