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: rs139961185
rs139961185
SIK3
11 116936627 intron variant G/A snv 1.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs141023293
rs141023293
SIK3
1.000 0.120 11 116902201 intron variant G/A snv 1.5E-02
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs2044426
rs2044426
SIK3
1.000 0.040 11 116885467 intron variant G/A snv 7.1E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs78692246
rs78692246
SIK3
11 116920591 intron variant G/A snv 7.3E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs78692246
rs78692246
SIK3
11 116920591 intron variant G/A snv 7.3E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs12225230
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2012 2018
dbSNP: rs12225230
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12225230
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2018
dbSNP: rs10047462
rs10047462
SIK3 ; APOA1-AS
11 116851325 intron variant G/C;T snv
CUI: C3541318
Disease: Soluble Transferrin Receptor Measurement
Soluble Transferrin Receptor Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2075292
rs2075292
SIK3
11 116861796 intron variant G/T snv 0.80 0.86
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2008 2019
dbSNP: rs12279433
rs12279433
SIK3
1.000 0.040 11 116877505 intron variant G/T snv 7.1E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs7115583
rs7115583
SIK3
11 116913660 intron variant G/T snv 0.17
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10892044
rs10892044
SIK3
1.000 0.040 11 116896183 intron variant T/C snv 0.16
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs11216186
rs11216186
SIK3
1.000 0.040 11 116913976 intron variant T/C snv 7.5E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2018 2018
dbSNP: rs77204473
rs77204473
SIK3
11 116934348 intron variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs77204473
rs77204473
SIK3
11 116934348 intron variant T/C;G snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs11216185
rs11216185
SIK3
1.000 0.040 11 116912258 intron variant T/G snv 7.5E-02
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		0.800 1.000 1 2012 2012